. . . . . . . . . . . . "[The great majority of cases of the Hutchinson-Gilford progeroid syndrome (HGPS) (Progeria of Childhood'') are caused by a single nucleotide mutation (1824 C->T) in the LMNA gene which encodes lamin A and C, nuclear intermediate filaments that are important components of the nuclear lamina.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2016-02-19"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2016-05-13T12:45:39+02:00"^^ . . . . . . . . . . . "v4.0.0.0" . "v4.0.0" .