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]. The gene discussed is PKP2; the disease is Arrhythmogenic right ventricular dysplasia.