Distinct clustering of point mutations in mitochondrial DNA among patients with mitochondrial encephalomyopathies and with Parkinson's disease
- 30 April 1991
- journal article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 176 (2) , 938-946
- https://doi.org/10.1016/s0006-291x(05)80276-1
Abstract
No abstract availableKeywords
Funding Information
- Ministry of Health, Labour and Welfare
- Ministry of Education, Culture, Sports, Science and Technology (01-02-39)
This publication has 24 references indexed in Scilit:
- Quantitative determination of deleted mitochondrial DNA relative to normal DNA in parkinsonian striatum by a kinetic PCR analysisBiochemical and Biophysical Research Communications, 1990
- Increase of deleted mitochondrial DNA in the striatum in Parkinson's disease and senescenceBiochemical and Biophysical Research Communications, 1990
- Mechanistic studies of ionizing radiation and oxidative mutagenesis: genetic effects of a single 8-hydroxyguanine (7-hydro-8-oxoguanine) residue inserted at a unique site in a viral genomeBiochemistry, 1990
- Mitochondrial Myopathy Caused by Long-Term Zidovudine TherapyNew England Journal of Medicine, 1990
- Direct sequencing of deleted mitochondrial DNA in myopathic patientsBiochemical and Biophysical Research Communications, 1989
- Mitochondrial DNA Mutation Associated with Leber's Hereditary Optic NeuropathyScience, 1988
- Maternal inheritance of deleted mitochondrial DNA in a family with mitochondrial myopathyBiochemical and Biophysical Research Communications, 1988
- Photolabelling of a mitochondrially encoded subunit of NADH dehydrogenase with [3H]dihydrorotenoneFEBS Letters, 1987
- Mitochondrial DNA and human evolutionNature, 1987
- Complete sequence of bovine mitochondrial DNA conserved features of the mammalian mitochondrial genomeJournal of Molecular Biology, 1982