LMNA mutations have been associated with several clinically distinct neuromuscular disorders including Emery-Dreifuss muscular dystrophy, limb girdle muscular dystrophy type 1B and Charcot-Marie-Tooth diseases type 2B1 [38]–[40]. Here, LMNA is linked to Autosomal dominant limb-girdle muscular dystrophy type 1B.