It has been reported that LMNA mutations can cause autosomal forms of Emery-Dreifuss muscular dystrophy (AD-EDMD) and limb-girdle muscular dystrophy type 1B (LGMD1B), which show clinical features of proximal dominant muscle weakness [9, 32]. Here, LMNA is linked to Autosomal dominant limb-girdle muscular dystrophy type 1B.