Inherited and de novo mutations in the cardiac actin gene cause hypertrophic cardiomyopathy

Journal of Molecular and Cellular Cardiology

Volumn 32, Issue 9, 2000, Pages 1687-1694

  Olson, Timothy M ^a   Doan, Thao P ^a   Kishimoto, Nina Y ^a   Whitby, Frank G ^a   Ackerman, Michael J ^b   Fananapazir, Lameh ^c  

^a UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

^b MAYO CLINIC   (United States)

^c NATIONAL HEART LUNG AND BLOOD INSTITUTE   (United States)

Author keywords

Actin; Cardiomyopathy; Genetics; Molecular biology; Mutation

Indexed keywords

ACTIN;

ADULT; AMINO ACID SUBSTITUTION; ARTICLE; CONGESTIVE HEART FAILURE; GENE MUTATION; HUMAN; HUMAN TISSUE; HYPERTROPHIC CARDIOMYOPATHY; MISSENSE MUTATION; PRIORITY JOURNAL; PROTEIN EXPRESSION; SARCOMERE; SCHOOL CHILD;

EID: 0033799445     PISSN: 00222828     EISSN: None     Source Type: Journal    
DOI: 10.1006/jmcc.2000.1204     Document Type: Article

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