Mutations in lamins, particularly in the LMNA gene, can cause a broad range of diseases such as Hutchinson-Gilford Progeria Syndrome (HGPS), Emery-Dreifuss Muscular Dystrophy, and autosomal dominant leukodystrophy, collectively referred to as laminopathies (Charar and Gruenbaum, 2017; Wong and Stewart, 2020). Here, LMNA is linked to Hutchinson-Gilford progeria syndrome.