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

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Bibliographic Details
Published in:Human molecular genetics Vol. 16; no. 11; pp. 1307 - 1318
Main Authors: 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
Format: Journal Article
Language:English
Published: Oxford Oxford University Press 2007
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ISSN:0964-6906
1460-2083