iPSC-based models have been established for a range of muscular dystrophies and laminopathies, including Limb–Girdle muscular dystrophy [34], Duchenne muscular dystrophy [35], Hutchinson–Gilford progeria syndrome, or dilated cardiomyopathy [36], and also for EDMD type 2 (laminopathy caused by a mutation in the LMNA gene encoding lamin A/C) [37,38]. This evidence concerns the gene LMNA and muscular dystrophy.