. . . . . . . . . . . . "[Our study confirmed that the p.R225X mutation leads to cardiac conduction disease with late or no development of DCM, underscoring the importance of this mutation in putative familial `lone conduction disease.` Nearly one third of LMNA mutation carriers had experienced a thromboembolic event.]. 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 . "2014-10-02T12:38:03+02:00"^^ . . . . . . . . . . . "v2.1.0.0" . "v2.1.0" .