Since then more DCM-associated mutations were identified in the LMNA gene (Forleo et al., 2015; Haas et al., 2015; Pérez-Serra et al., 2015; Ambrosi et al., 2016; Hasselberg et al., 2017; Kayvanpour et al., 2017; Walsh et al., 2017). This evidence concerns the gene LMNA and familial dilated cardiomyopathy.