Both of them are regulators of RyR2[15] and mutations in both triadin and calmodulin have been associated with catecholaminergic polymorphic ventricular tachycardia, a rare familial arrhythmogenic disorder characterized by maligant ventricular arrhythmias and increased risk of SCD[16, 17]. Here, RYR2 is linked to catecholaminergic polymorphic ventricular tachycardia.