
Clinical impact of the TPM1 p.Tyr221Cys variant causing hypertrophic cardiomyopathy


Hypertrophic cardiomyopathy (HCM) is a relatively common (about 1 in 500 in the general population) inherited cardiac condition characterized by hypertrophy of the left ventricle wall, usually the septum, not explained by other conditions. The most severe forms can be responsible for sudden cardiac death.
