. . . . . . . "[analysis of mutations in the GJB2 gene in Brazilian families with either familial or sporadic deafness in order to determine the frequency and type of connexin26 mutations among patients with non-syndromic hearing loss]. 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" .