. . . . . . . . . . . . "[Five novel missense DES mutations including the first localized to the highly conserved 1A domain were detected in 6 subjects (1.4%) Mutations in the 1A helical domain, as well as the 2B rod domain, are capable of causing a dilated cardiomyopathy phenotype ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2009-03-31"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2014-10-02T12:33:05+02:00"^^ . . . . . . . . . . . "v2.1.0.0" . "v2.1.0" .