Mitochondrial tRNAlle mutation in fatal cardiomyopathy
- 15 July 1992
- journal article
- case report
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 186 (1) , 47-53
- https://doi.org/10.1016/s0006-291x(05)80773-9
Abstract
No abstract availableKeywords
Funding Information
- Ministry of Education, Culture, Sports, Science and Technology
- Ministry of Health, Labour and Welfare
This publication has 10 references indexed in Scilit:
- A new mtDNA mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS)Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 1991
- Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNALeu(UUR)The Lancet, 1991
- Mitochondrial tRNAthr mutation in fatal infantile respiratory enzyme deficiencyBiochemical and Biophysical Research Communications, 1991
- Mutations in mitochondrial tRNA genes: a frequent cause of neuromuscular diseasesNucleic Acids Research, 1991
- Mitochondrial mutation in fatal infantile cardiomyopathyThe Lancet, 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 muscle mitochondrial DNA in patients with mitochondrial myopathiesNature, 1988
- Cloning of human mitochondrial DNA in Escherichia coliJournal of Molecular Biology, 1980
- Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Nature, 1970