In particular, RYR2 has previously been reported as gene associated with several arrhythmic diseases, including LQTS [38], catecholaminergic polymorphic ventricular tachycardia (CPVT) [39–41], arrhythmogenic right ventricular dysplasia type 2 [42–44] and sudden infant death syndrome [45]. The gene discussed is RYR2; the disease is familial long QT syndrome.