. . . . . . . . . . . . "[Here, we present a patient with Opitz G/BBB syndrome and a unique MID1 gene point mutation c.1703T . . . . . "2014-02-25"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2014-10-02T12:36:04+02:00"^^ . . . . . . . . . . . "v2.1.0.0" . "v2.1.0" .