A novel TPM1 mutation in a family with hypertrophic cardiomyopathy and sudden cardiac death in childhood.

Van Driest SL, Will ML, Atkins DL, Ackerman MJ
Am J Cardiol. 2002 90 (10): 1123-7

PMID: 12423715 · DOI:10.1016/s0002-9149(02)02780-7

MeSH Terms (15)

Adult Cardiomyopathy, Hypertrophic Child Child, Preschool Death, Sudden, Cardiac Diagnosis, Differential Echocardiography Female Genetic Predisposition to Disease Genetic Testing Humans Male Pedigree Point Mutation Tropomyosin

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