A Glimpse Into Multigene Rare Variant Genetics. Triple Mutations in Hypertrophic Cardiomyopathy

Journal of the American College of Cardiology

Volumn 55, Issue 14, 2010, Pages 1454-1455

  Hershberger, Ray E ^a  

^a UNIVERSITY OF MIAMI MILLER SCHOOL OF MEDICINE   (United States)

Author keywords

complex genotypes; genetics; hypertrophic cardiomyopathy; outcome

Indexed keywords

AMINO ACID; MYOSIN HEAVY CHAIN BETA;

BLOOD PRESSURE; CARDIOVASCULAR DISEASE; CLINICAL FEATURE; CONGESTIVE CARDIOMYOPATHY; DIET; DISEASE CLASSIFICATION; DISEASE COURSE; DISEASE SEVERITY; EDITORIAL; ETHNICITY; GENE MUTATION; GENETIC DISORDER; GENETIC SCREENING; GENETIC VARIABILITY; HUMAN; HYPERTROPHIC CARDIOMYOPATHY; LONG QT SYNDROME; MISSENSE MUTATION; MULTIGENE FAMILY; NONSENSE MUTATION; PHENOTYPE; PRIORITY JOURNAL; RISK FACTOR; SYMPTOM;

CARDIOMYOPATHY, HYPERTROPHIC; HUMANS; MUTATION; PEDIGREE;

EID: 77949898544     PISSN: 07351097     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jacc.2009.12.025     Document Type: Editorial

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