Most ARVC cases are associated with mutations in desmosomal genes, including plakophilin-2 (PKP2), desmoglein-2 (DSG2), desmocollin-2 (DSC2), plakoglobin (JUP), and desmoplakin (DSP) (Dalal et al., 2005). The gene discussed is PKP2; the disease is Arrhythmogenic right ventricular dysplasia.