Mitochondrial leucine tRNA mutation in neurological diseases
Open Access
- 13 April 1991
- journal article
- other
- Published by Elsevier in The Lancet
- Vol. 337 (8746) , 927-928
- https://doi.org/10.1016/0140-6736(91)90272-q
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Mitochondrial leucine tRNA mutation in a mitochondrial encephalomyopathyThe Lancet, 1991
- A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathiesNature, 1990
- Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNALys mutationCell, 1990
- Preferential amplification and molecular characterization of junction sequences of a pathogenetic deletion in human mitochondrial DNAGenomics, 1989
- Directly repeated sequences associated with pathogenic mitochondrial DNA deletions.Proceedings of the National Academy of Sciences, 1989