. . . . . . . . . . . . "[Based on these data, we hypothesize that Cx26 profound hearing loss may be not always congenital, with the possibility of an early window of functional time before the final defect is established.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2016-02-19"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2016-05-13T12:46:12+02:00"^^ . . . . . . . . . . . "v4.0.0.0" . "v4.0.0" .