J A Morgan-Hughes1. Show Affiliations » 1. Institute of Neurology, London, UK.
Abstract
Mesh: See more » Chromosome DeletionDNA, Mitochondrial/geneticsGenetic Carrier ScreeningHumansMitochondrial Myopathies/geneticsMitochondrial Myopathies/pathologyMuscles/pathologyMutationPhenotype
Substances: See more » DNA, Mitochondrial
Year: 1994 PMID: 7804467 DOI: 10.1097/00019052-199410000-00014
Source DB: PubMed Journal: Curr Opin Neurol ISSN: 1350-7540 Impact factor: 5.710