No evidence of genetic heterogeneity in dominant optic atrophy.-Reference-Cited by-同舟云学术

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No evidence of genetic heterogeneity in dominant optic atrophy.

Published:1995-12-01 Issue:12 Volume:32 Page:951-953
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Bonneau D,Souied E,Gerber S,Rozet J M,D'Haens E,Journel H,Plessis G,Weissenbach J,Munnich A,Kaplan J

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference11 articles.

1. Optic atrophy;Went, L.N.,1990

2. Congenital optic atrophy with dominant mode of inheritance. A clinical and genetic study of;Kjer, P.;Acta Ophthalmol Suppl; Danish families,19

3. Diagnostic criteria in dominantly inherited juvenile optic atrophy. A report of 3 new families;Smith, D.P.,1972

4. Dominant optic atrophy. The clinical profile;Kline, L.S.; Glaser, J.S.;Arch Ophthalmol,1979

5. Autosomal dominant optic atrophy. A spectrum of disability;Hoyt, C.S.;Ophthalmology,1980

Cited by 29 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Dominant optic atrophy: Culprit mitochondria in the optic nerve;Progress in Retinal and Eye Research;2021-07

2. Physiological evidence for impairment in autosomal dominant optic atrophy at the pre-ganglion level;Graefe's Archive for Clinical and Experimental Ophthalmology;2012-08-04

3. Dominant optic atrophy;Orphanet Journal of Rare Diseases;2012

4. OPA1 expression in the human retina and optic nerve;Experimental Eye Research;2006-11

5. Clinical Heterogeneity of Hereditary Optic Atrophy in a Turkish Family;Neuro-Ophthalmology;2005-01

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