Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathy

Proceedings of the National Academy of Sciences of the United States of America

Volumn 89, Issue 23, 1992, Pages 11164-11168

  Yoneda, Makoto ^a   Chomyn, Anne ^a   Martinuzzi, Andrea ^a   Hurko, Orest ^b   Attardi, Giuseppe ^a  

^a CALIFORNIA INSTITUTE OF TECHNOLOGY   (United States)

^b JOHNS HOPKINS UNIVERSITY   (United States)

Author keywords

Encephalopathy; Lactic acidosis; Mitochondrial myopathy; Stroke like episodes

Indexed keywords

LACTIC ACID; MITOCHONDRIAL DNA;

ADULT; ARTICLE; BLAST TRANSFORMATION; CHILD; CLINICAL ARTICLE; DNA DETERMINATION; DNA REPLICATION; ENCEPHALOMYOPATHY; FEMALE; GENOTYPE; HUMAN; HUMAN CELL; LACTIC ACIDOSIS; MALE; MUTANT; MYOBLAST; PEDIGREE; POINT MUTATION; PRIORITY JOURNAL; STROKE;

CELL DIVISION; CELLS, CULTURED; CLONING, MOLECULAR; DNA REPLICATION; DNA, MITOCHONDRIAL; HUMAN; IN VITRO; MITOCHONDRIAL ENCEPHALOMYOPATHIES; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0026457825     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.89.23.11164     Document Type: Article

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