LMNA and Autosomal dominant limb-girdle muscular dystrophy type 1B: LMNA mutations cause a plethora of diseases called laminopathies, of which three forms affect skeletal muscle (Maggi et al., 2016): limb-girdle muscular dystrophy type 1B (LGMD1B), autosomal dominant Emery-Dreifuss muscular dystrophy 2 (EDMD2), and LMNA-related congenital muscular dystrophy (L-CMD).