Opa1 deficiency in a mouse model of autosomal dominant optic atrophy impairs mitochondrial morphology, optic nerve structure and visual function-Reference-Cited by-同舟云学术

Opa1 deficiency in a mouse model of autosomal dominant optic atrophy impairs mitochondrial morphology, optic nerve structure and visual function

Published:2007-04-11 Issue:11 Volume:16 Page:1307-1318
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Davies Vanessa J.,Hollins Andrew J.,Piechota Malgorzata J.,Yip Wanfen,Davies Jennifer R.,White Kathryn E.,Nicols Phillip P.,Boulton Michael E.,Votruba Marcela

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/16/11/1307/6950248/ddm079.pdf

Reference53 articles.

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2. Dominant optic atrophy. The clinical profile;Kline;Arch. Ophthalmol.,1979

3. Clinical features, molecular genetics, and pathophysiology of dominant optic atrophy;Votruba;J. Med. Genet.,1998

4. A clinicopathologic study of autosomal dominant optic atrophy;Johnston;Am. J. Ophthalmol.,1979

5. Clinical features in affected individuals from 21 pedigrees with dominant optic atrophy;Votruba;Arch. Ophthalmol.,1998

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