Mutations in the LMNA gene cause a diverse group of diseases known as laminopathies which include, among others, dilated cardiomyopathy (DCM) type 1A, Emery–Dreifuss muscular dystrophy type 2 and type 3, limb–girdle muscular dystrophy type 1B, Dunnigan-type familial partial lipodystrophy, Charcot–Marie–Tooth disease type 2B1 and Hutchinson–Gilford progeria syndrome (HGPS) [8]. Here, LMNA is linked to dilated cardiomyopathy.