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

Connections (1)

This publication is referenced by other Labnodes entities:

Links