Association of 25 bp Deletion in MYBPC3 Gene with Left Ventricle Dysfunction in Coronary Artery Disease Patients

MYBPC3 gene variations in hypertrophic cardiomyopathy patients in India

(2011) Reena R. Tanjore et al.   CANADIAN JOURNAL OF CARDIOLOGY

A frameshift deletion mutation in the cardiac myosin-binding protein C gene associated with dilated phase of hypertrophic cardiomyopathy and dilated cardiomyopathy

(2010) Nobuhiko Hitomi et al.   Journal of Cardiology

Molecular basis of hereditary cardiomyopathy: abnormalities in calcium sensitivity, stretch response, stress response and beyond

(2010) Akinori Kimura   JOURNAL OF HUMAN GENETICS

Sarcomere Mutations in Cardiomyopathy With Left Ventricular Hypertrabeculation

(2009) Lisa M. Dellefave et al.   Circulation-Cardiovascular Genetics

Ethnicity-related differences in left ventricular function, structure and geometry: a population study of UK Indian Asian and European white subjects

(2009) N. S. Chahal et al.   HEART

A common MYBPC3 (cardiac myosin binding protein C) variant associated with cardiomyopathies in South Asia

(2009) Perundurai S Dhandapany et al.   NATURE GENETICS