Mitochondrial DNA mutations in human degenerative diseases and aging
- 24 May 1995
- journal article
- research article
- Published by Elsevier BV in Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
- Vol. 1271 (1), 141-151
- https://doi.org/10.1016/0925-4439(95)00021-u
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- Mitochondrial diabetes revisitedNature Genetics, 1994
- An ND-6 mitochondrial DNA mutation associated with leber hereditary optic neuropathyBiochemical and Biophysical Research Communications, 1992
- Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletionNature Genetics, 1992
- Leber's hereditary optic neuropathy and complex I deficiency in muscleAnnals of Neurology, 1991
- Porin interaction with hexokinase and glycerol kinase: Metabolic microcompartmentation at the outer mitochondrial membraneBiochemical Medicine and Metabolic Biology, 1991
- Deletion mutants are functionally dominant over wild-type mitochondrial genomes in skeletal muscle fiber segments in mitochondrial diseaseCell, 1990
- Detection of hydroxyl radical in the mitochondria of ischemic-reperfused myocardium by trapping with salicylateBiochemical and Biophysical Research Communications, 1989
- A Mitochondrial DNA Mutation as a Cause of Leber's Hereditary Optic NeuropathyThe New England Journal of Medicine, 1989
- DECLINE IN SKELETAL MUSCLE MITOCHONDRIAL RESPIRATORY CHAIN FUNCTION: POSSIBLE FACTOR IN AGEINGThe Lancet, 1989
- Mitochondrial DNA Mutation Associated with Leber's Hereditary Optic NeuropathyScience, 1988