One of the most prominent forms of progeria is HGPS [2], which is caused by a single point mutation (c.1824C > T; G608G) in exon 11 of the LMNA gene, resulting in the alternatively spliced mRNA and subsequent production of the mutant lamin A protein progerin [1,2]. The gene discussed is LMNA; the disease is Hutchinson-Gilford progeria syndrome.