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

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

Van Driest, Sara L; Vasile, Vlad C; Ommen, Steve R; Will, Melissa L; Tajik, A Jamil; Gersh, Bernard J; Ackerman, Michael J.

Affiliation

Van Driest SL; Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic College of Medicine, Rochester, Minnesota, USA.

J Am Coll Cardiol ; 44(9): 1903-10, 2004 Nov 02.

Article in En | MEDLINE | ID: mdl-15519027

Subject(s)

Cardiomyopathy, Hypertrophic/genetics; Carrier Proteins/genetics; Heterozygote; Mutation/genetics; Adolescent; Adult; Aged; Aged, 80 and over; Child; Child, Preschool; Exons/genetics; Family Health; Female; Genetic Predisposition to Disease/genetics; Humans; Infant; Infant, Newborn; Male; Middle Aged; Minnesota; Pedigree; Phenotype; Sarcomeres/genetics; Statistics as Topic; Troponin I/genetics; Troponin T/genetics

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Collection: 01-internacional Database: MEDLINE Main subject: Cardiomyopathy, Hypertrophic / Carrier Proteins / Heterozygote / Mutation Type of study: Prognostic_studies Limits: Adolescent / Adult / Aged / Aged80 / Child / Child, preschool / Female / Humans / Infant / Male Country/Region as subject: America do norte Language: En Journal: J Am Coll Cardiol Year: 2004 Type: Article Affiliation country: United States

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