A novel frameshift mutation of SMPX causes a rare form of X-linked nonsyndromic hearing loss in a Chinese family. (Q30354540)
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English | A novel frameshift mutation of SMPX causes a rare form of X-linked nonsyndromic hearing loss in a Chinese family. |
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A novel frameshift mutation of SMPX causes a rare form of X-linked nonsyndromic hearing loss in a Chinese family. (English)
1 reference
Lingyun Mei
Jie Sun
Xueping Wang
Juncheng Wang
Zhengmao Hu
Yunpeng Dong
Hongsheng Chen
Chufeng He
Yalan Liu
Xuezhong Liu
25 May 2017
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