. . . . . . . "[one-third (3 out of 9) autosomal dominant low frequency sensorineural hearing loss (LFSNHL) families had mutations in WFS1, indicating that in non-syndromic hearing loss WFS1 is restrictively & commonly found within autosomal dominant LFSNHL families]. 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 . "2017-10-17T13:17:18+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .