. . . . . . . . . . . . "[HGPS is almost always caused by a de novo point mutation in the lamin A gene (LMNA) that activates a cryptic splice donor site, producing a truncated mutant protein termed `progerin.` WT prelamin A is anchored to the nuclear envelope by a farnesyl isoprenoid lipid.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2014-02-25"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2014-10-02T12:33:31+02:00"^^ . . . . . . . . . . . "v2.1.0.0" . "v2.1.0" .