Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy

Journal of the American College of Cardiology

Volumn 44, Issue 9, 2004, Pages 1903-1910

  Van Driest, Sara L ^a   Vasile, Vlad C ^a   Ommen, Steve R ^b   Will, Melissa L ^a   Tajik, A Jamil ^b   Gersh, Bernard J ^b   Ackerman, Michael J ^a,b,c  

^a MAYO CLINIC   (United States)

^b Mayo Clinic   (United States)

^c 200 First St SW Rochester M   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; MYOSIN BINDING PROTEIN C;

ADULT; ARTICLE; CLINICAL FEATURE; COHORT ANALYSIS; CONTROLLED STUDY; DNA SEQUENCE; FEMALE; GENE MUTATION; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; HYPERTROPHIC CARDIOMYOPATHY; MAJOR CLINICAL STUDY; MALE; MEDICAL RECORD; PHENOTYPE; PRIORITY JOURNAL;

ADOLESCENT; ADULT; AGED; AGED, 80 AND OVER; CARDIOMYOPATHY, HYPERTROPHIC; CARRIER PROTEINS; CHILD; CHILD, PRESCHOOL; EXONS; FAMILY HEALTH; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HETEROZYGOTE; HUMANS; INFANT; INFANT, NEWBORN; MALE; MIDDLE AGED; MINNESOTA; MUTATION; PEDIGREE; PHENOTYPE; SARCOMERES; STATISTICS; TROPONIN I; TROPONIN T;

EID: 7044264544     PISSN: 07351097     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jacc.2004.07.045     Document Type: Article

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