. . . . . . . . . . . . "[Genetic research has identified the cause of syndromic forms of PDA, such as the TFAP2B mutations in Char syndrome.]. 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 . "2014-10-02T12:39:31+02:00"^^ . . . . . . . . . . . "v2.1.0.0" . "v2.1.0" .