The nuclear lamins have historically received substantial attention due to the number of mutations (as of 31 January 2020, nearly 500 different mutations have been identified in the human LMNA gene, http://www.umd.be/LMNA/ accessed on 28 December 2021) and their association with several devastating human diseases called laminopathies [13,14,15]. The gene discussed is LMNA; the disease is laminopathy.