"MYH7-V878A and CACNA1C-A1594V mutations were detected in a Chinese Family with Hypertrophic Cardiomyopathy. Among those with only the MYH7-V878A mutation subject III-7 showed abnormal ECG recordings asymmetric septal hypertrophy and myocardial fibrosis and subjects II-13 and III-15 showed some abnormal repolarization borderline LV wall thickness and normal cardiac magnetic resonance (CMR) findings."xsd:string