ORCA
Online Research @ Cardiff
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Davies, Vanessa J., Powell, Kathryn A., White, Kathryn E., Yip, Wan Fen, Hogan, Vanessa, Hollins, Andrew John  ORCID: https://orcid.org/0000-0002-0324-9376, Davies, Jennifer Rhian, Piechota, Malgorzata, Brownstein, David G., Moat, Stuart James, Nichols, Philip P., Wride, Michael A., Boulton, Michael Edwin and Votruba, Marcela ORCID: https://orcid.org/0000-0002-7680-9135
2008.
A missense mutation in the murine Opa3 gene models human Costeff syndrome.
Brain
131
(2)
, pp. 368-380.
10.1093/brain/awm333
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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
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