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A novel splicing variant in the TMC1 gene causes non-syndromic hearing loss in a Chinese family
oleh: Beiping Zeng, Hongen Xu, Yongan Tian, Qianyu Lin, Haifeng Feng, Zhifeng Zhang, Siqi Li, Wenxue Tang, Lishao Guo
Format: | Article |
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Diterbitkan: | Wolters Kluwer 2022-11-01 |
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