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
Subjects:	Biological and medical sciences Fundamental and applied biological sciences. Psychology Genetics of eukaryotes. Biological and molecular evolution Molecular and cellular biology Animal model Optic nerve Deficiency Rodentia Autosome Atrophy Vertebrata Mitochondria Mammalia Visual pathway Mouse Morphology Genetics Structure
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