. . . . . . . "[investigation of 9 Usher syndrome type 2 families from Quebec & New Brunswick; seven USH2A mutations were identified in eight patients; one of them, c.4338 _ 4339delCT, accounts for 10 out of 18 disease alleles]. 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 . "2017-10-17T13:17:10+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .