D R Johns. Show Affiliations »
Abstract
Entities: Disease Mutation
Mesh: See more » DNA, Mitochondrial/geneticsHumansMutationOptic Atrophies, Hereditary/diagnosisOptic Atrophies, Hereditary/genetics
Substances: See more » DNA, Mitochondrial
Year: 1990 PMID: 2222273 DOI: 10.1001/archopht.1990.01070120053027
Source DB: PubMed Journal: Arch Ophthalmol ISSN: 0003-9950