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Mutations in theWFS1gene are a frequent cause of autosomal dominant nonsyndromic low-frequency hearing loss in Japanese

✍ Scribed by Hisakuni Fukuoka; Yukihiko Kanda; Shuji Ohta; Shin-ichi Usami

Publisher: Nature Publishing Group
Year: 2007
Tongue: English
Weight: 187 KB
Volume: 52
Category: Article
ISSN: 1435-232X
DOI: 10.1007/s10038-007-0144-3

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