For instance, the 960delT mutation in the LMNA gene may be manifested as primary DCM, or DCM associated with either Emery-Dreifuss muscular Dystrophy (EDMD)-like or limb girdle muscular dystrophy (LGMD)-like phenotype (Brodsky et al., 2000). The gene discussed is LMNA; the disease is limb-girdle muscular dystrophy.