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Novel ACTG1 mutation causing autosomal dominant non-syndromic hearing impairment in a Chinese family

✍ Scribed by Ping Liu; Hu Li; Xiang Ren; Haiyan Mao; Qihui Zhu; Zhengfeng Zhu; Rong Yang; Wenlin Yuan; Jingyu Liu; Qing Wang; Mugen Liu

Book ID: 118651183
Publisher: Elsevier
Year: 2008
Tongue: Chinese
Weight: 713 KB
Volume: 35
Category: Article
ISSN: 1673-8527
DOI: 10.1016/s1673-8527(08)60075-2

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