The lamin intermediate filament (IF) proteins are the primary structural proteins of the nuclear lamina. Their numerous functions include maintenance of nuclear shape and structure, transcription regulation, nuclear pore positioning, heterochromatin organization, and downstream pathways including differentiation, proliferation, and senescence. [1][2][3] Lamins are type V intermediate filament proteins, subdivided into A and B types. Mutations in the genes encoding these proteins, the majority of which occur in LMNA (encoding lamin A/C), are associated with a group of rare heterogeneous diseases known as laminopathies. Laminopathies comprise a growing list of diseases with