. . . . . . . "[Mother and daughter with KID Syndrome with vertical transmaission of a mutation 148G -- > A in GJB2 (D50N)/two cases with combined sensorineural and conductive hearing loss suggesting the Cx26 D50N mutation can cause latter.]. 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 . "2017-10-17T13:12:59+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .