Growing old: the most common mitochondrial disease of all?
- 1 December 1992
- journal article
- Published by Springer Nature in Nature Genetics
- Vol. 2 (4) , 251-252
- https://doi.org/10.1038/ng1292-251
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- Mitochondrial DNA deletions in human brain: regional variability and increase with advanced ageNature Genetics, 1992
- Mosaicism for a specific somatic mitochondrial DNA mutation in adult human brainNature Genetics, 1992
- DISEASES OF THE MITOCHONDRIAL DNAAnnual Review of Biochemistry, 1992
- Quantitation of a mitochondrial DNA deletion in Parkinson's diseaseFEBS Letters, 1992
- An introduction to the free radical hypothesis in Parkinson's diseaseAnnals of Neurology, 1992
- Regulation of mitochondrial gene expression in mammalian cellsBiochemical Society Transactions, 1990
- Widespread tissue distribution of mitochondrial DNA deletions in Kearns‐Sayre syndromeNeurology, 1990
- Mitochondrial mutations may increase oxidative stress: Implications for carcinogenesis and aging?Free Radical Biology & Medicine, 1990
- DECLINE IN SKELETAL MUSCLE MITOCHONDRIAL RESPIRATORY CHAIN FUNCTION: POSSIBLE FACTOR IN AGEINGPublished by Elsevier ,1989
- MITOCHONDRIAL DNA MUTATIONS AS AN IMPORTANT CONTRIBUTOR TO AGEING AND DEGENERATIVE DISEASESThe Lancet, 1989