. . . . . . . . . . . . "[In our studies, about 36.9% infants hearing loss cases can be found the mutations in SLC26A4 and GJB2 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2013-07-06"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2014-10-02T12:32:19+02:00"^^ . . . . . . . . . . . "v2.1.0.0" . "v2.1.0" .