RBM20 and muscular dystrophy: These genes include AKAP6, CFL2, MYH6, MYH7, MYO18B, MYO1C, MYOCD, MYOT, MYOZ1, MYPN, PKP2, RBM20, SGCA, SSPN, SYNPO2L, TTN, TTN-AS, and WIPF1. Two genes, RBM20 and PKP2, have been associated with more specific cardiac conditions, dilated cardiomyopathy [100] and arrhythmogenic right ventricular cardiomyopathy [101], respectively, while the gene SCGC is associated with the skeletal muscle condition, muscular dystrophy [102].