Mitochondrial DNA mutations and neuromuscular disease
- PMID: 2652392
- DOI: 10.1016/0168-9525(89)90005-x
Mitochondrial DNA mutations and neuromuscular disease
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.
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