Heidi Lumish,Mark V. Sherrid,Paul M.L. Janssen,Giovanni Ferrari,Kohei Hasegawa,Estíbaliz Castillero,Elizabeth Adlestein,Daniel G. Swistel,Veli K. Topkara,Matthew J. Maurer,Muredach P. Reilly,Yuichi J. Shimada
Hypertrophic cardiomyopathy (HCM) is the most common genetic cardiac disease. Signaling pathways that link genetic sequence variants to clinically overt HCM and progression to severe forms of HCM remain unknown.