Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenance. (2008)

First Author: Hudson G

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1093/brain/awm272

PubMed Identifier: 18065439

Publication URI: http://europepmc.org/abstract/MED/18065439

Type: Journal Article/Review

Volume: 131

Parent Publication: Brain : a journal of neurology

Issue: Pt 2

ISSN: 0006-8950