| Literature DB >> 2652392 |
Abstract
Mitochondrial DNA mutations have been identified in patients with certain neuromuscular diseases. Point mutations have been associated with maternally inherited diseases, while deletions have been identified in some 'spontaneous' cases.Entities:
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Year: 1989 PMID: 2652392 DOI: 10.1016/0168-9525(89)90005-x
Source DB: PubMed Journal: Trends Genet ISSN: 0168-9525 Impact factor: 11.639