TP53 and Miyoshi myopathy: Previous studies reported general MM hypomethylation accompanied by hypermethylation of specific genes such glutathione peroxidase 3, TP53 (Hurt et al., 2006), CDNK2B, DAPK (Dimopoulos, Gimsing, and Grønbæk, 2014), p15, and p16 (Ng et al., 1997).