1994 William Allan Award Address. Mitochondrial DNA variation in human evolution, degenerative disease, and aging.
- 1 August 1995
- journal article
- Vol. 57 (2) , 201-23
Abstract
No abstract availableThis publication has 98 references indexed in Scilit:
- Disequilibrium of multiple DNA markers on the human Y chromosomeAnnals of Human Genetics, 1992
- 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
- Cytochrome b mutations in Leber hereditary optic neuropathyBiochemical 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
- Y chromosome DNA polymorphisms in human populations: differences between Caucasoids and Africans detected by 49a and 49f probesAnnals of Human Genetics, 1990
- Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre SyndromeNew England Journal of Medicine, 1989
- Mitochondrial DNA Mutation Associated with Leber's Hereditary Optic NeuropathyScience, 1988
- Mitochondrial DNA and human evolutionNature, 1987
- Maternal inheritance of human mitochondrial DNA.Proceedings of the National Academy of Sciences, 1980