Familial mitochondrial encephalomyopathy (MERRF): Genetic, pathophysiological, and biochemical characterization of a mitochondrial DNA disease

Cell

Volumn 55, Issue 4, 1988, Pages 601-610

  Wallace, Douglas C ^a   Zheng, Xianxian ^a   Lott, Marie T ^a   Shoffner, John M ^a   Hodge, Judith A ^a   Kelley, Richard I ^b   Epstein, Charles M ^a   Hopkins, Linton C ^a  

^a EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CLINICAL ARTICLE; CONTROLLED STUDY; DNA DAMAGE; ENCEPHALOMYOPATHY; ETHNIC OR RACIAL ASPECTS; GENETIC DISORDER; HUMAN; HUMAN CELL; MITOCHONDRION; PRIORITY JOURNAL;

CALORIMETRY, INDIRECT; DNA, MITOCHONDRIAL; HUMAN; MAGNETIC RESONANCE SPECTROSCOPY; MUTATION; OXIDATIVE PHOSPHORYLATION; OXYGEN CONSUMPTION; PEDIGREE; PHENOTYPE; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0024163051     PISSN: 00928674     EISSN: None     Source Type: Journal    
DOI: 10.1016/0092-8674(88)90218-8     Document Type: Article

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