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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

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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

Publisher: Oxford University Press

URL: http://dx.doi.org/10.1093/hmg/ddm079

DOI: 10.1093/hmg/ddm079


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