M D Brown. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » HumansMitochondria/physiologyMitochondrial Encephalomyopathies/pathologyOptic Atrophies, Hereditary/pathology
Year: 1999 PMID: 10426138 DOI: 10.1016/s0022-510x(99)00087-8
Source DB: PubMed Journal: J Neurol Sci ISSN: 0022-510X Impact factor: 3.181