Mitochondrial DNA variation in human evolution and disease

Gene

Volumn 238, Issue 1, 1999, Pages 211-230

  Wallace, Douglas C ^a   Brown, Michael D ^a   Lott, Marie T ^a  

^a EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Leber's hereditary optic neuropathy; Mitochondrial disease; Mitochondrial DNA; mtDNA mutation

Indexed keywords

MITOCHONDRIAL DNA;

DISORDERS OF MITOCHONDRIAL FUNCTIONS; EVOLUTION; GENE MUTATION; HAPLOTYPE; HUMAN; MITOCHONDRION; MOLECULAR EVOLUTION; PHYLOGENY; POPULATION GENETICS; PRIORITY JOURNAL; REVIEW;

EID: 0032833421     PISSN: 03781119     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0378-1119(99)00295-4     Document Type: Article

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