N J Volpe, S Lessell. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » DNA, Mitochondrial/geneticsHumansMutation/geneticsOptic Atrophies, Hereditary/geneticsOptic Atrophies, Hereditary/pathologyOptic Atrophies, Hereditary/therapyPhenotype
Substances: See more » DNA, Mitochondrial
Year: 1993 PMID: 8325730 DOI: 10.1097/00004397-199303320-00015
Source DB: PubMed Journal: Int Ophthalmol Clin ISSN: 0020-8167