A point mutation in the cytb gene of cardiac mtDNA associated with complex III deficiency in ischemic cardiomyopathy

Biochemistry and Molecular Biology International

Volumn 40, Issue 3, 1996, Pages 487-495

  Marin Garcia, Jose ^a   Hu, Yaping ^a   Ananthakrishnan, Radha ^a   Pierpont, Mary Ella ^b   Pierpont, Gordon L ^b   Goldenthal, Michael J ^a  

^a Molecular Cardiology Institute   (United States)

^b UNIVERSITY OF MINNESOTA MEDICAL SCHOOL   (United States)

Author keywords

Cardiomyopathy; Mitochondrial DNA; Myocardial ischemia

Indexed keywords

CYTOCHROME B; HEART ENZYME; MITOCHONDRIAL DNA; MUTANT PROTEIN; UBIQUINOL CYTOCHROME C REDUCTASE;

ADULT; AMINO ACID SUBSTITUTION; ARTICLE; CARDIOMYOPATHY; CLINICAL ARTICLE; CONTROLLED STUDY; ENZYME ACTIVITY; ENZYME DEFICIENCY; ENZYME STRUCTURE; FEMALE; HEART MUSCLE; HEART MUSCLE ISCHEMIA; HEART MUSCLE METABOLISM; HUMAN; HUMAN TISSUE; MALE; POINT MUTATION; STRUCTURE ACTIVITY RELATION;

EID: 0029955977     PISSN: 10399712     EISSN: None     Source Type: Journal    
DOI: 10.1080/15216549600201053     Document Type: Article

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