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

Davies, Vanessa J., Hollins, Andrew John ORCID: https://orcid.org/0000-0002-0324-9376, Piechota, Malgorzata, Yip, Wan Fen, Davies, Jennifer Rhian, White, Kathryn, Nicols, Phillip, Boulton, Michael Edwin and Votruba, Marcela ORCID: https://orcid.org/0000-0002-7680-9135 2007. Opa1 deficiency in a mouse model of autosomal dominant optic atrophy impairs mitochondrial morphology, optic nerve structure and visual function. Human Molecular Genetics 16 (11) , pp. 1307-1318. 10.1093/hmg/ddm079

Full text not available from this repository.

Item Type:	Article
Date Type:	Publication
Status:	Published
Schools:	Optometry and Vision Sciences Neuroscience and Mental Health Research Institute (NMHRI)
Publisher:	Oxford University Press
ISSN:	0964-6906
Last Modified:	05 Feb 2025 22:48
URI:	https://orca.cardiff.ac.uk/id/eprint/883

Citation Data

Cited 318 times in Scopus. View in Scopus. Powered By Scopus® Data

Actions (repository staff only)

Edit Item