MOLECULAR BASIS OF MITOCHONDRIAL MYOPATHIES
- 16 April 1988
- journal article
- other
- Published by Elsevier in The Lancet
- Vol. 331 (8590) , 884-885
- https://doi.org/10.1016/s0140-6736(88)91631-5
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
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- Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathiesNature, 1988
- Six unidentified reading frames of human mitochondrial DNA encode components of the respiratory-chain NADH dehydrogenaseNature, 1985
- Deficiency in ubiquinone cytochrome c reductase in a patient with mitochondrial myopathy and lactic acidosis.Proceedings of the National Academy of Sciences, 1983
- Sequence and organization of the human mitochondrial genomeNature, 1981
- A MITOCHONDRIAL MYOPATHY CHARACTERIZED BY A DEFICIENCY IN REDUCIBLE CYTOCHROME bBrain, 1977