Mitochondrial encephalomyopathies with the mutation of the mitochondrial tRNALeu(UUR) gene
- 31 January 1992
- journal article
- case report
- Published by Elsevier BV in The Journal of Pediatrics
- Vol. 120 (1), 62-66
- https://doi.org/10.1016/s0022-3476(05)80599-2
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- A point mutation in the mitochondrial tRNALeu(UUR) gene in melas (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes)Biochemical and Biophysical Research Communications, 1990
- 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
- Deletions of mitochondrial DNA in Kearns‐Sayre syndromeNeurology, 1988
- MELAS syndromeNeurology, 1988
- Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathiesNature, 1988
- Mitochondrial myopathiesAnnals of Neurology, 1985
- Maternally inherited mitochondrial myopathy and myoclonic epilepsyAnnals of Neurology, 1985
- Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndromeAnnals of Neurology, 1984
- Sequence and organization of the human mitochondrial genomeNature, 1981