Mutations in LMNA manifest as such varied disorders as muscular dystrophies, lipodystrophies, dermopathies, cardiomyopathies, and progeria syndromes, including Hutchinson-Gilford progeria (HGPS; OMIM ID# 176670) [1], [2], [8]–[10]. This evidence concerns the gene LMNA and Hutchinson-Gilford progeria syndrome.