Genetic, clinical, molecular, and pathogenic aspects of the South Asian-specific polymorphic MYBPC3(Delta25bp) variant.
Hypertrophic cardiomyopathy (HCM) is a cardiac genetic disease characterized by ventricular enlargement, diastolic dysfunction, and increased risk for sudden cardiac death. Sarcomeric genetic defects are the predominant known cause of HCM. In particular, ..... Read More