Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy.

Van Driest SL, Vasile VC, Ommen SR, Will ML, Tajik AJ, Gersh BJ, Ackerman MJ
J Am Coll Cardiol. 2004 44 (9): 1903-10

PMID: 15519027 · DOI:10.1016/j.jacc.2004.07.045

MeSH Terms (26)

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 as Topic Troponin I Troponin T

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