. . . . . . . . . . . . "[Mutations in GJB2, encoding the gap junction beta-2 protein Connexin 26, are associated with autosomal recessive nonsyndromic sensorineural hearing loss (NSHL), autosomal dominant NSHL, and several forms of syndromic sensorineural 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 . "2014-10-02T12:33:11+02:00"^^ . . . . . . . . . . . "v2.1.0.0" . "v2.1.0" .