Mitochondrial DNA mutations and neuromuscular disease
- 1 January 1989
- journal article
- review article
- Published by Elsevier in Trends in Genetics
- Vol. 5 (1) , 9-13
- https://doi.org/10.1016/0168-9525(89)90005-x
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- Mitochondrial DNA Mutation Associated with Leber's Hereditary Optic NeuropathyScience, 1988
- Mitochondrial DNA in anucleate human blood cellsBiochemical and Biophysical Research Communications, 1988
- Maternal inheritance of deleted mitochondrial DNA in a family with mitochondrial myopathyBiochemical and Biophysical Research Communications, 1988
- Mitochondrial myopathies and respiratory chain proteinsTrends in Biochemical Sciences, 1988
- Conformational mutations in human mitochondrial DNANature, 1987
- The search for mitochondrial inheritance of human diseasesTrends in Genetics, 1985
- Maternally inherited mitochondrial myopathy and myoclonic epilepsyAnnals of Neurology, 1985
- NADH-CoQ REDUCTASE DEFICIENT MYOPATHY: SUCCESSFUL TREATMENT WITH RIBOFLAVINThe Lancet, 1983
- Complete sequence of bovine mitochondrial DNA conserved features of the mammalian mitochondrial genomeJournal of Molecular Biology, 1982
- Tissue‐specific genes code for polypeptide VIa of bovine liver and heart cytochrome c oxidaseFEBS Letters, 1982