Mitochondrial leucine tRNA mutation in a mitochondrial encephalomyopathy
- 26 January 1991
- journal article
- other
- Published by Elsevier in The Lancet
- Vol. 337 (8735) , 234-235
- https://doi.org/10.1016/0140-6736(91)92196-9
Abstract
No abstract availableFunding Information
- Ministry of Education and Science
This publication has 5 references indexed in Scilit:
- Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNALys mutationCell, 1990
- Multiple populations of deleted mitochondrial DNA detected by a novel gene amplification methodBiochemical and Biophysical Research Communications, 1989
- Disproportionate Deficiency of Iron-Sulfur Clusters and Subunits of Complex I in Mitochondrial EncephalomyopathyPediatric Research, 1989
- Maternal inheritance of deleted mitochondrial DNA in a family with mitochondrial myopathyBiochemical and Biophysical Research Communications, 1988
- Deficiency of subunits of complex I and mitochondrial encephalomyopathyAnnals of Neurology, 1988