There have been mutations in several genes identified as associated with human ARVC, in particular, mutations in the five desmosomal genes—desmoplakin, plakophilin 2, desmoglein 2, desmocollin 2, and junction plakoglobin (DSP, PKP2, DSG2, DSC2, and JUP) [84]. Here, DSC2 is linked to Arrhythmogenic right ventricular dysplasia.