J B Kerrison, V Biousse, N J Newman. Show Affiliations »
Abstract
Entities: Disease Mutation
Mesh: See more » AdolescentAtaxia/geneticsAtaxia/pathologyDNA, Mitochondrial/geneticsHumansMitochondrial Myopathies/geneticsMitochondrial Myopathies/pathologyNervous System Diseases/geneticsNervous System Diseases/pathologyPoint MutationRetinitis Pigmentosa/geneticsRetinitis Pigmentosa/pathologySyndrome
Substances: See more » DNA, Mitochondrial
Year: 2000 PMID: 10676807 DOI: 10.1001/archopht.118.2.298
Source DB: PubMed Journal: Arch Ophthalmol ISSN: 0003-9950