. . . . . . . "[To determinate the frequency of digenic (GJB2/GJB6) background of DFNB (autosomal recessive non-syndromic hearing loss), 17 patients with heterozygous 35delG mutation were screened for deletion of 342 kb in GJB6 gene, and none found.]. 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" .