A novel TPM1 mutation in a family with hypertrophic cardiomyopathy and sudden cardiac death in childhood
Author/Authors :
Van Driest، نويسنده , , Sara L and Will، نويسنده , , Melissa L and Atkins، نويسنده , , Dianne L and Ackerman، نويسنده , , Michael J، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2002
Pages :
5
From page :
1123
To page :
1127
Abstract :
We sought to define the pathogenic mutation in a family with hypertrophic cardiomyopathy (HC) and a markedly arrhythmogenic phenotype. The proband was an 8-year-old female with a sentinel event of sudden death. Screening echocardiograms revealed HC in 2 o
