MTTOCHONDRIAL DNA DELETION IN ENCEPHALOMYOPATHY
- 26 November 1988
- journal article
- other
- Published by Elsevier in The Lancet
- Vol. 332 (8622) , 1253-1254
- https://doi.org/10.1016/s0140-6736(88)90847-1
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Maternal inheritance of deleted mitochondrial DNA in a family with mitochondrial myopathyBiochemical and Biophysical Research Communications, 1988
- DELETIONS OF MUSCLE MITOCHONDRIAL DNAThe Lancet, 1988
- KEARNS-SAYRE SYNDROME WITH MUSCLE MITOCHONDRIAL DNA DELETIONThe Lancet, 1988
- 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
- Sequence and organization of the human mitochondrial genomeNature, 1981