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Journal articles on the topic 'Leberis'

Author: Grafiati

Published: 3 June 2025

Last updated: 31 July 2025

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1

KOTOV, ALEXEY A., and JUAN M. FUENTES-REINÉS. "A new species of Leberis Smirnov, 1989 (Cladocera: Chydoridae) from Colombia." Zootaxa 3957, no. 5 (2015): 553. http://dx.doi.org/10.11646/zootaxa.3957.5.4.

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A new species of Leberis Smirnov 1989 (Cladocera: Chydoridae) is described based on the material from Ciénaga El Convento (Atlántico Department), Ciénaga Grande de Santa Marta (Magdalena Department), and Laguna Navío Quebrado (La Guajira Department), Colombia. In the Neotropics, Leberis colombiensis sp. nov. could be confused with L. davidi Richard, 1985. But the former differs from the latter in: (1) smaller size; (2) smaller post-pore distance; (3) gonopore region on male postabdomen un-inflated, not overhanging base of postabdominal claw; (4) shorter postanal portion of male postabdomen. Di

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Kotov, Alexey A., and Juan M. Fuentes-Reinés. "A new species of Leberis Smirnov, 1989 (Cladocera: Chydoridae) from Colombia." Zootaxa 3957, no. 5 (2015): 553–66. https://doi.org/10.11646/zootaxa.3957.5.4.

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3

Neretina, Anna N., and Artem Y. Sinev. "A revision of the genus Leberis Smirnov, 1989 (Cladocera: Chydoridae) in the Old World and Australia." Zootaxa 4079, no. 5 (2016): 501–33. https://doi.org/10.11646/zootaxa.4079.5.1.

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Neretina, Anna N., Sinev, Artem Y. (2016): A revision of the genus Leberis Smirnov, 1989 (Cladocera: Chydoridae) in the Old World and Australia. Zootaxa 4079 (5): 501-533, DOI: 10.11646/zootaxa.4079.5.1

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4

Sousa, Francisco Diogo Rocha, Lourdes Maria Abdu Elmoor-Loureiro, and Sandro Santos. "Position of the dentifera-group in the Coronatella-branch and its relocation to a new genus: Magnospina gen. n. (Crustacea, Chydoridae, Aloninae)." ZooKeys 586 (May 4, 2016): 95–119. https://doi.org/10.3897/zookeys.586.8209.

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Magnospina gen. n. was created to relocate species of the dentifera-group from Alona sensu lato (Crustacea: Cladocera) and include Magnospina dentifera comb. n. and Magnospina siamensis comb. n. The synapomorphies of the Magnospina gen. n. are (1) basal spines longer than 2/3 of the postabdominal claw, (2) presence of 1–4 large denticles, broad at their bases, protruding downwards, without setules between them. Morphological traits such as habitus, rostrum and postabdomen shape, armature of IDL setae, number of setae on the exopod of limb III are also important in the distinction between Magno

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SINEV, ARTEM Y., and LA-ORSRI SANOAMUANG. "Hormonal induction of males as a method for studying tropical cladocerans: description of males of four chydorid species (Cladocera: Anomopoda: Chydoridae)." Zootaxa 2826, no. 1 (2011): 45. http://dx.doi.org/10.11646/zootaxa.2826.1.2.

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Methyl farnesoate, a crustacean juvenile hormone, successfully induced male development in several littoral cladocerans from Thailand in short-term multispecies cultures. Male morphology is fully described in four species of Chydoridae— Oxyurella singalensis Daday, 1898, Leberis diaphanus (King, 1853), Leydigia cf. ciliata Gauthier, 1939, Disparalona cf. hamata (Birge, 1910). Males of the latter two taxa from Thailand differ from these from the other localities, suggesting the presence of sibling-species in the Indochina region.

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SINEV, ARTEM Y., and MARCELO SILVA-BRIANO. "Cladocerans of genus Alona Baird, 1843 (Cladocera: Anomopoda: Chydoridae) and related genera from Aguascalientes State, Mexico." Zootaxa 3569, no. 1 (2012): 1. http://dx.doi.org/10.11646/zootaxa.3569.1.1.

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Eight cladoceran species of Alona s. lato and related genera were found in Aguascalientes state, Mexico, after extensivesampling efforts. Two of them are new for science. Both new species belong to the pulchella-group of Alona and sharedistinctive features of the group. Alona aguascalientensis sp. nov. differs from the other species of the group by thepresence of denticles on posteroventral corner of valves, by a moderately elongated narrow postabdomen with weaklyprotruding distal angle and postanal marginal denticles of the same size, and by the morphology of major head pores, withconnection

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7

DE SOUSA, JEAN RIBEIRO M., GILMAR PERBICHE-NEVES, CARLOS E. F. ROCHA, ELIANA A. PANARELLI, LOURDES M. A. ELMOOR-LOUREIRO, and FRANCISCO DIOGO ROCHA SOUSA. "Richness and composition of Cladocera (Crustacea: Branchiopoda) in Brazilian rupestrian cerrados, with comments on distribution and taxonomy." Zootaxa 5219, no. 2 (2022): 139–52. http://dx.doi.org/10.11646/zootaxa.5219.2.3.

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Several studies that involve a faunal survey of Cladocera in Brazil have been carried out in recent years; however, knowledge of the distribution and diversity of species of this group in semiterrestrial and aquatic bodies of rupestrian cerrado is still rare. The present study evaluated the richness and composition of cladoceran species in these environments in the central parts of the country. Samples were collected at nine sites of rupestrian cerrado from 2011 to 2012. In total, 47 cladocerans species were identified, belonging to six families, emphasizing the Chydoridae family with the grea

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8

VAN DAMME, KAY, and HENRI J. DUMONT. "Further division of Alona Baird, 1843: separation and position of Coronatella Dybowski & Grochowski and Ovalona gen.n. (Crustacea: Cladocera)." Zootaxa 1960, no. 1 (2008): 1–44. http://dx.doi.org/10.11646/zootaxa.1960.1.1.

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We investigate morphology and taxonomic rank of several Alona species related to A. rectangula Sars, 1861. Despite high morphological intraspecific variability, a number of synapomorphies shows that taxa related to A. rectangula are sufficiently different in external and internal morphology from “true” Alona Baird, 1843. These are removed from Alona into separate genera. The rare West-African A. holdeni Green 1962 is redescribed and we describe a new species from North Africa, Arabia and islands in the Western Indian Ocean. We reinstate the name Coronatella Dybowski & Grochowski to receive

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9

NERETINA, ANNA N., and ARTEM Y. SINEV. "A revision of the genus Leberis Smirnov, 1989 (Cladocera: Chydoridae) in the Old World and Australia." Zootaxa 4079, no. 5 (2016): 501. http://dx.doi.org/10.11646/zootaxa.4079.5.1.

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10

ELÍAS-GUTIÉRREZ, MANUEL, FERNANDO MARTÍNEZ JERÓNIMO, NATALIA V. IVANOVA, MARTHA VALDEZ-MORENO, and PAUL D. N. HEBERT. "DNA barcodes for Cladocera and Copepoda from Mexico and Guatemala, highlights and new discoveries." Zootaxa 1839, no. 1 (2008): 1. http://dx.doi.org/10.11646/zootaxa.1839.1.1.

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DNA barcoding, based on sequence diversity in the mitochondrial COI gene, has proven an excellent tool for identifying species in many animal groups. Here, we report the first barcode studies for freshwater zooplankton from Mexico and Guatemala and discuss the taxonomic and biological implications of this work. Our studies examined 61 species of Cladocera and 21 of Copepoda, about 40% of the known fauna in this region. Sequence divergences among conspecific individuals of cladocerans and copepods averaged 0.82% and 0.79%, respectively, while sequence divergences among congeneric taxa were on a

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11

Chuprov, Aleksandr D., Ekaterina A. Pidodniy, Tat’yana V. Kazakova, and Ol’ga V. Marshinskaya. "Search for New Laboratory Methods for Diagnostics of Leber’s Hereditary Optic Neuropathy." NAUKA MOLODYKH (Eruditio Juvenium) 13, no. 1 (2025): 113–26. https://doi.org/10.23888/hmj2025131113-126.

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INTRODUCTION: Determination and validation of specific and reliable diagnostic criteria for mitochondrial diseases, in particular, Leber’s hereditary optic neuropathy, is becoming an urgent need of the scientific community. In this context, the development and optimization of patients’ examination protocols indicating disorders in the functional state of the mitochondrial respiratory chain components are relevant in the laboratory diagnostics. AIM: To characterize the main metabolic changes in an organism in mitochondrial dysfunction. In the review, modern data on the main metabolic changes in

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12

Ermolaeva, E. V., E. E. Sidorenko, V. S. Malinovskaya, et al. "Modern diagnosis and treatment of Leber congenital amaurosis with CEP290 gene." Russian ophthalmology of children 50, no. 4 (2024): 27–37. https://doi.org/10.25276/2307-6658-2024-4-27-37.

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Purpose. Demonstration of a clinical case of Leber congenital amaurosis. Material and methods. This article presents a clinical case of diagnosing Leber congenital amaurosis in a 5-year-old patient. Results. The disease is caused by biallelic loss-offunction mutations in the CEP290 gene (Leber congenital amaurosis type 10), which leads to dysregulation of metabolism within photoreceptor ciliary transport. A heterozygous mutation in the 26th intron of the CEP290 gene (chr12: 88494960T>C, rs281865192) leads to the formation of an alternative splicing site (c.2991+1655A>G, NM_025114.3), whi

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13

Warady, Bradley A., Gerhard Cibis, Uri Alon, Douglas Blowey, and Stanley Hellerstein. "Senior-Loken Syndrome: Revisited." Pediatrics 94, no. 1 (1994): 111–12. http://dx.doi.org/10.1542/peds.94.1.111.

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The combination of familial juvenile nephronophthisis (FJN) and congenital amaurosis of Leber, the so called Senior-Loken Syndrome, was first described by Senior et al in 1961.1 Despite recognition of the syndrome for &gt; 30 years, its occurrence is relatively rare and the basis for the oculorenal association remains unresolved. Our recent experience with two patients who had end-stage renal disease (ESRD) as a manifestation of the syndrome prompted this review. CASE HISTORIES A.M. is an 11-year-old girl who complained of generalized fatigue over the previous 3 weeks. The patient had been

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14

Seedorff, Tove. "LEBER'S DISEASE." Acta Ophthalmologica 46, no. 1 (2009): 4–25. http://dx.doi.org/10.1111/j.1755-3768.1968.tb02490.x.

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15

Alves Andrade, Diana, Beatriz Morais Pinto, Cristiana Reis, Catarina Côrte-Real, and Maria Inês Costa. "Sudden Decrease in Visual Acuity – An Atypical Case." Eurasian Journal of Family Medicine 14, no. 2 (2025): 84–86. https://doi.org/10.33880/ejfm.2025140206.

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Leber's hereditary optic neuropathy is a rare disease resulting from mutations in the mitochondrial DNA. It is characterized by rapidly progressive, painless vision loss, with development of a central visual scotoma. This case describes a woman with no significant personal or family medical history except for active smoking and occasional cannabinoid use. She sought care at her family health unit due to sudden worsening of visual acuity in her right eye, with progressively worsening blurred vision that had developed over the course of four days. Despite the exhaustive diagnostic evaluation, th

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16

Bardelli, A. M., L. Biagini, and L. Barberi. "Leber's optic neuritis." Ophthalmic Paediatrics and Genetics 5, no. 3 (1985): 133–40. http://dx.doi.org/10.3109/13816818509006124.

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17

Seedorff, Tove. "LEBER'S DISEASE II." Acta Ophthalmologica 46, no. 5 (2009): 985–92. http://dx.doi.org/10.1111/j.1755-3768.1968.tb00937.x.

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18

SEEDORFF, TOVE. "LEBER's DISEASE IV." Acta Ophthalmologica 47, no. 4 (2009): 813–21. http://dx.doi.org/10.1111/j.1755-3768.1969.tb03707.x.

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19

SEEDORFF, TOVE. "LEBER's DISEASE III." Acta Ophthalmologica 47, no. 1 (2009): 23–29. http://dx.doi.org/10.1111/j.1755-3768.1969.tb05606.x.

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20

SEEDORFF, TOVE. "LEBER'S DISEASE V." Acta Ophthalmologica 48, no. 2 (2009): 186–213. http://dx.doi.org/10.1111/j.1755-3768.1970.tb08189.x.

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21

Skalka, H. "Leber's congenital amaurosis." British Journal of Ophthalmology 69, no. 5 (1985): 396. http://dx.doi.org/10.1136/bjo.69.5.396.

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22

Skalka, H. "Leber's congenital amaurosis." British Journal of Ophthalmology 69, no. 5 (1985): 396. http://dx.doi.org/10.1136/bjo.69.5.396-a.

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23

Schroeder, Robert. "Leber's Congenital Amaurosis." Archives of Ophthalmology 105, no. 3 (1987): 356. http://dx.doi.org/10.1001/archopht.1987.01060030076030.

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24

Joshi, Stuti, and Allan Kermode. "048 Harding’s disease: an important MS mimic." Journal of Neurology, Neurosurgery & Psychiatry 90, e7 (2019): A16.2—A16. http://dx.doi.org/10.1136/jnnp-2019-anzan.43.

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IntroductionLeber’s hereditary optic neuropathy is a mitochondrially-inherited disorder characterized by bilateral, painless visual loss, which leads to severe optic atrophy.1 LHON can be associated with an MS-like illness referred to as Harding’s disease.2We report two siblings, who both harbour the 11778 mtDNA mutation, but manifest markedly different clinical phenotypes; a male with classical LHON and a female with Harding’s disease.Methods and ResultsA 61-year-old female, who was diagnosed with MS 22 years ago was referred to our service for a second opinion. She developed unilateral painl

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25

Nikoskelainen, E. K., R. J. Marttila, K. Huoponen, et al. "Leber's "plus": neurological abnormalities in patients with Leber's hereditary optic neuropathy." Journal of Neurology, Neurosurgery & Psychiatry 59, no. 2 (1995): 160–64. http://dx.doi.org/10.1136/jnnp.59.2.160.

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26

Rościszewska-Żukowska, Iwona, and Halina Bartosik-Psujek. "Demyelinating or hereditary optic neuropathy? Comparison of selected disease entities." Aktualności Neurologiczne 20, no. 2 (2020): 82–87. http://dx.doi.org/10.15557/an.2020.0011.

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The paper discusses retrobulbar optic neuritis secondary to multiple sclerosis, Leber’s hereditary optic neuropathy, and Leber’s hereditary optic neuropathy with multiple sclerosis-like disease – Harding’s syndrome. Retrobulbar optic neuritis secondary to multiple sclerosis is the most common disease (neuropathy) of the optic nerve in young adults and often the first clinical manifestation of multiple sclerosis. Despite a characteristic triad of symptoms and evident focal demyelination in brain magnetic resonance, misdiagnoses still occur. Leber’s hereditary optic neuropathy (atrophy) is a gen

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27

Tecellioglu, Mehmet, A. Ozcan, and Hatice Tosun. "Multiple sclerosis associated with lebers hereditary optic neuropathy: a case report / Leber'in herediter optik noropatisi ve multipl skleroz birlikteligi: olgu sunumu." Journal of Turgut Ozal Medical Center 23, no. 2 (2016): 239. http://dx.doi.org/10.5455/jtomc.2015.3242.

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28

Berninger, T. A., A. C. Bird, and G. B. Arden. "Leber's hereditary optic atrophy." Ophthalmic Paediatrics and Genetics 10, no. 3 (1989): 211–27. http://dx.doi.org/10.3109/13816818909009877.

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29

Low, Adeline, Yee Ling Neoh, Siu Wan Foo, and Azida J. Kadir. "Leber’s hereditary optic neuropathy." Malaysian Journal of Ophthalmology 2, no. 4 (2020): 281–87. http://dx.doi.org/10.35119/myjo.v2i4.88.

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Leber’s hereditary optic neuropathy (LHON) is a maternally inherited mitochondrial disease caused by several point mutations in mitochondrial DNA. We present the case of a healthy 12-year-old Chinese boy who presented with bilateral, painless, subacute loss of central vision (more severe in the left eye the than right eye) for 1 week. No abnormalities were detected on magnetic resonance imaging of the brain and orbit. Serial Humphrey visual field tests initially showed a centrocaecal scotoma that worsened progressively. Cerebrospinal fluid samples and blood investigations showed normal results

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30

Maslova, N. N., Ye A. Andreyeva, and Ye V. Yerokhina. "LEBER'S DISEASE. CLINICAL CASE." Bulletin of Siberian Medicine 12, no. 5 (2013): 126–32. http://dx.doi.org/10.20538/1682-0363-2013-5-126-132.

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Violation of visual functions and oculomotor frustration develop at 90% of patients with MS. More than a half of patients are transferred by the numerous recurrence of an optical neuritis which is coming to an end with a partial atrophy of optic nerve. For well-timed purpose of pathogenetic treatment differential diagnostics with other diseases, being accompanied an atrophy of an optic nerve, in particular with Leber's disease.

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31

Millichap, J. Gordon. "Atypical Leber’s Optic Neuropathy." Pediatric Neurology Briefs 7, no. 5 (1993): 37. http://dx.doi.org/10.15844/pedneurbriefs-7-5-8.

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32

Volpe, Nicholas J., та Simmons Lessell. "Leberʼs Hereditary Optic Neuropathy". International Ophthalmology Clinics 33, № 2 (1993): 153–68. http://dx.doi.org/10.1097/00004397-199303320-00015.

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33

Neetens, A., and R. M. Smets. "Leber's neurogenic stellate maculopathy." Neuro-Ophthalmology 7, no. 6 (1987): 315–28. http://dx.doi.org/10.3109/01658108708996010.

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34

Cherninkova, S. "Leber’s hereditary optic neuropathy." Bulgarian Review of Ophthalmology 61, no. 2 (2017): 41. http://dx.doi.org/10.14748/bro.v0i2.4514.

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35

Skarote, Mary Ann, Roanne E. Flom та Louise A. Doyle. "LEBERʼS IDIOPATHIC STELLATE NEURORETINITIS". Optometry and Vision Science 72, SUPPLEMENT (1995): 58. http://dx.doi.org/10.1097/00006324-199512001-00089.

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36

Johns, Donald R., Kyle H. Smith, Peter J. Savino, and Neil R. Miller. "Leber's Hereditary Optic Neuropathy." Ophthalmology 100, no. 7 (1993): 981–86. http://dx.doi.org/10.1016/s0161-6420(93)31527-7.

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37

Bi, Rui, A. Mei Zhang, and Yong-Gang Yao. "Leber's Hereditary Optic Neuropathy." Ophthalmology 118, no. 7 (2011): 1489–1489. http://dx.doi.org/10.1016/j.ophtha.2011.04.007.

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38

Pahor, Dušica. "Leber's idiopathic stellate neuroretinitis." Canadian Journal of Ophthalmology 36, no. 6 (2001): 347–49. http://dx.doi.org/10.1016/s0008-4182(01)80124-1.

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39

Jay, Barrie. "Leber's hereditary optic neuropathy." Eye 4, no. 3 (1990): vii. http://dx.doi.org/10.1038/eye.1990.52.

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40

Sadun, Alfredo A., Chiara La Morgia, and Valerio Carelli. "Leber’s Hereditary Optic Neuropathy." Current Treatment Options in Neurology 13, no. 1 (2010): 109–17. http://dx.doi.org/10.1007/s11940-010-0100-y.

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41

Johns, Donald R. "Leber's Hereditary Optic Neuropathy." Archives of Ophthalmology 111, no. 4 (1993): 495. http://dx.doi.org/10.1001/archopht.1993.01090040087038.

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42

Johns, Donald R. "Leber's Hereditary Optic Neuropathy." Archives of Ophthalmology 110, no. 11 (1992): 1577. http://dx.doi.org/10.1001/archopht.1992.01080230077025.

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43

Newman, Nancy J. "Leber's Hereditary Optic Neuropathy." Archives of Neurology 50, no. 5 (1993): 540. http://dx.doi.org/10.1001/archneur.1993.00540050082021.

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44

Beganovic, Allen, and Vladislav Dzinic. "Leber’s Hereditary Optic Neuropathy." Medical Archives 79, no. 3 (2025): 241. https://doi.org/10.5455/medarh.2025.79.241-248.

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Background: Leber’s hereditary optic neuropathy (LHON) is the most common maternally inherited disease linked to mitochondrial DNA (mtDNA). The patients present with subacute asymmetric bilateral vision loss. It is a rare disease that typically affects young adults–men more than women–and is a relatively common cause of blindness. The majority (more than 95%) of patients have one of three mtDNA point mutations: m.14484T→C, m.3460G→A, or m.11778G→A.The hallmark of hereditary optic neuropathies determined by mitochondrial dysfunction is the vulnerability and degeneration of retinal ganglion cell

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45

Baniszewski, Julie, Nicole Miller, Eutychus M. Kariuki, James P. Cuda, and Emma N.I. Weeks. "Cricotopus lebetis intraspecific competition and damage to hydrilla." Florida Entomologist 103, no. 1 (2020): 32. https://doi.org/10.1653/024.103.0405.

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Baniszewski, Julie, Miller, Nicole, Kariuki, Eutychus M., Cuda, James P., Weeks, Emma N.I. (2020): Cricotopus lebetis intraspecific competition and damage to hydrilla. Florida Entomologist 103 (1): 32, DOI: 10.1653/024.103.0405, URL: https://bioone.org/journals/florida-entomologist/volume-103/issue-1/024.103.0405/Cricotopus-lebetis-Intraspecific-Competition-and-Damage-to-Hydrilla/10.1653/024.103.0405.full

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46

Teive, Hélio Afonso Ghizoni, André Ribeiro Troiano, Salmo Raskin, and Lineu César Werneck. "Leber's hereditary optic neuropathy: case report and literature review." Sao Paulo Medical Journal 122, no. 6 (2004): 276–79. http://dx.doi.org/10.1590/s1516-31802004000600010.

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CONTEXT: Leber's hereditary optic neuropathy is an important cause of progressive painless visual loss among young male patients. OBJECTIVE: To report on a case of a young patient with a clinical and neurophysiological condition suggestive of Leber's hereditary optic neuropathy, confirmed by genetic testing. CASE REPORT: We describe a 17-year-old male with progressive bilateral visual loss. Two maternal uncles had had similar patterns of visual loss. The patient had a history of smoking and alcohol abuse. Neuro-ophthalmological examination revealed visual acuity of 20/800 in both eyes, with de

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47

WANG, YU, DAOCHAO JIN, and JIANJUN GUO. "Water mites of the genus Lebertia Neuman (Acari: Hydrachnidia: Lebertiidae) from China, with description of three new species." Zootaxa 5399, no. 3 (2024): 231–40. http://dx.doi.org/10.11646/zootaxa.5399.3.2.

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Three new water mite species of the genus Lebertia Neuman, 1880—Lebertia (Lebertia) gimina sp. nov., Lebertia (Mixolebertia) dinghuensis sp. nov. and Lebertia (Mixolebertia) wuyiensis sp. nov.—are described from China, along with one new Chinese record—Lebertia (Lebertia) ignatowi Sokolow, 1930. The key characteristics for the subgenera of Lebertia are given.

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48

Zhang, Yong, Jia-jia Yuan, Hong-li Liu, Zhen Tian, Si-wei Liu, and Bin Li. "Three Cases of Leber’s Hereditary Optic Neuropathy with Rapid Increase in Visual Acuity After Gene Therapy." Current Gene Therapy 19, no. 2 (2019): 134–38. http://dx.doi.org/10.2174/1566523219666190618094505.

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Background: During the first few trials of gene therapy for Leber’s hereditary optic neuropathy performed by our group, the visual acuity of the patients increased gradually over several months, or even years. However, in the current round of gene therapy for Leber’s hereditary optic neuropathy, we noted that the visual acuity of three patients increased rapidly, within a few days after treatment. Case presentation: Three patients who were diagnosed with mitochondrial gene 11778 mutation (associated with a G-to-A transition at Mt-11778 in the ND4 subunit gene of complex I of mitochondrial DNA

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49

Wang, Yu, Jialin Wang, Daochao Jin, and Jianjun Guo. "Taxonomic notes on water mites of the genus Lebertia (Acari, Hydrachnidiae, Lebertiidae) from China." Systematic and Applied Acarology 25, no. 1 (2020): 17–30. http://dx.doi.org/10.11158/saa.25.1.2.

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Of the genus Lebertia Neuman, 1880 (Acari, Hydrachnidiae, Lebertiidae), three subgenera, Septlebertia, Mixolebertia and Eolebertia, and the species Lebertia (Septlebertia) convergella Tuzovskij, 1990 are recorded for the first time from China. Four species new to science are described and illustrated: Lebertia (Mixolebertia) xuanensis sp. nov., Lebertia (s. str.) borealis sp. nov., Lebertia (s. str.) maolanensis sp. nov., and Lebertia (Eolebertia) exceedia sp. nov. A key is provided to the known Chinese species of the genus Lebertia.

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Traboulsi, Elias I., and Irene H. Maumenee. "Photoaversion in Leber's congenital amaurosis." Ophthalmic Genetics 16, no. 1 (1995): 27–30. http://dx.doi.org/10.3109/13816819509057851.

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