. . . . . . . . . . . . "[There was significant phenotypic variability, but the presence of skeletal muscle involvement (p < 0.001), supraventricular arrhythmia (p = 0.003), conduction defects (p = 0.01), and `mildly` DCM (p = 0.006) were predictors of LMNA mutations.]. 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 . "2014-10-02T12:37:25+02:00"^^ . . . . . . . . . . . "v2.1.0.0" . "v2.1.0" .