. . . . . . . . . . . . "[In this study, seventy-five Iranian families segregating autosomal recessive non-syndromic hearing impairment were analyzed/sequencing all 23 coding exons of TECTA, a frameshift mutation was 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 . "2015-08-25T14:39:25+02:00"^^ . . . . . . . . . . . "v3.0.0.0" . "v3.0.0" .