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Opa1 deficiency in a mouse model of autosomal dominant optic atrophy impairs mitochondrial morphology, optic nerve structure and visual function
Lookup NU author(s)
Dr Kathryn White
Dr Philip Nichols
Author(s)
Davies VJ, Hollins AJ, Piechota MJ, Yip W, Davies JR, White KE, Nichols PP, Boulton ME, Votruba M
Publication type
Article
Journal
Human Molecular Genetics
Year
2007
Volume
16
Issue
11
Pages
1307-1318
ISSN (print)
0964-6906
ISSN (electronic)
1460-2083
Full text for this publication is not currently held within this repository. Alternative links are provided below where available.
Publisher
Oxford University Press
URL
http://dx.doi.org/10.1093/hmg/ddm079
DOI
10.1093/hmg/ddm079
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