Publication | Open Access

Hypertrophic cardiomyopathy-linked mutation in troponin T causes myofibrillar disarray and pro-arrhythmic action potential changes in human iPSC cardiomyocytes

Cardiac MuscleCardiomyopathyMyofibrillar DisarrayHypertrophic Cardiomyopathy-linked MutationHuman Ipsc CardiomyocytesGeneticsPhysiologyMedicineCardiologyCardiovascular Genetics