Quantitation of mitochondrial DNA carrying tRNALys mutation in MERRF patients
- 16 September 1991
- journal article
- case report
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 179 (2) , 880-885
- https://doi.org/10.1016/0006-291x(91)91900-w
Abstract
No abstract availableKeywords
Funding Information
- Ministry of Education, Culture, Sports, Science and Technology (11-A, 2-A)
- Ministry of Health, Labour and Welfare
- National Center of Neurology and Psychiatry
This publication has 11 references indexed in Scilit:
- Mitochondrial DNA mutations in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)Biochemical and Biophysical Research Communications, 1991
- 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
- Identification of point mutations by mispairing PCR as exemplified in MERRF diseaseBiochemical 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
- Reactive site polymorphism in the murine protease inhibitor gene family is delineated using a modification of the PCR reaction (PCR + 1)Nucleic Acids Research, 1990
- Mitochondrial DNA Mutation Associated with Leber's Hereditary Optic NeuropathyScience, 1988
- Primer-Directed Enzymatic Amplification of DNA with a Thermostable DNA PolymeraseScience, 1988
- Sequence and organization of the human mitochondrial genomeNature, 1981
- Myoclonus epilepsy associated with ragged-red fibres (mitochondrial abnormalities): Disease entity or a syndrome?Journal of the Neurological Sciences, 1980