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Cardiac myosin binding protein–C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy

Cardiac MuscleCardiomyopathyHeart FailureCardiac MyosinCardiovascular DiseaseFamilial Hypertrophic CardiomyopathyGeneticsPathologyGene ExpressionMedicineCardiologyCardiovascular GeneticsCardiac Pathology