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Open Access
Peer-reviewed
Research Article
A novel frameshift mutation of SMPX causes a rare form of X-linked nonsyndromic hearing loss in a Chinese family
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Zhijie Niu,
Affiliations Department of Otolaryngology-Head and Neck Surgery, Xiangya Hospital, Central South University, Changsha, PR China, Key Laboratory of Otolaryngology Major Disease Research of Hunan Province, Changsha, PR China, Department of Otolaryngology (D-48), University of Miami Miller School of Medicine, Miami, FL, United States of America
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Yong Feng,
Affiliations Department of Otolaryngology-Head and Neck Surgery, Xiangya Hospital, Central South University, Changsha, PR China, Key Laboratory of Otolaryngology Major Disease Research of Hunan Province, Changsha, PR China, State Key Laboratory of Medical Genetics, Central South University, Changsha, PR China
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Lingyun Mei,
Affiliations Department of Otolaryngology-Head and Neck Surgery, Xiangya Hospital, Central South University, Changsha, PR China, Key Laboratory of Otolaryngology Major Disease Research of Hunan Province, Changsha, PR China
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Jie Sun,
Affiliations Department of Otolaryngology-Head and Neck Surgery, Xiangya Hospital, Central South University, Changsha, PR China, Key Laboratory of Otolaryngology Major Disease Research of Hunan Province, Changsha, PR China
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Xueping Wang,
Affiliations Department of Otolaryngology-Head and Neck Surgery, Xiangya Hospital, Central South University, Changsha, PR China, Key Laboratory of Otolaryngology Major Disease Research of Hunan Province, Changsha, PR China
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Juncheng Wang,
Affiliations Department of Otolaryngology-Head and Neck Surgery, Xiangya Hospital, Central South University, Changsha, PR China, Key Laboratory of Otolaryngology Major Disease Research of Hunan Province, Changsha, PR China
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Zhengmao Hu,
Affiliation State Key Laboratory of Medical Genetics, Central South University, Changsha, PR China
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Yunpeng Dong,
Affiliation Department of Otolaryngology (D-48), University of Miami Miller School of Medicine, Miami, FL, United States of America
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Hongsheng Chen,
Affiliations Department of Otolaryngology-Head and Neck Surgery, Xiangya Hospital, Central South University, Changsha, PR China, Key Laboratory of Otolaryngology Major Disease Research of Hunan Province, Changsha, PR China
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Chufeng He,
Affiliations Department of Otolaryngology-Head and Neck Surgery, Xiangya Hospital, Central South University, Changsha, PR China, Key Laboratory of Otolaryngology Major Disease Research of Hunan Province, Changsha, PR China
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Yalan Liu,
Affiliations Department of Otolaryngology-Head and Neck Surgery, Xiangya Hospital, Central South University, Changsha, PR China, Key Laboratory of Otolaryngology Major Disease Research of Hunan Province, Changsha, PR China
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Xinzhang Cai,
Affiliations Department of Otolaryngology-Head and Neck Surgery, Xiangya Hospital, Central South University, Changsha, PR China, Key Laboratory of Otolaryngology Major Disease Research of Hunan Province, Changsha, PR China
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Xuezhong Liu,
Affiliations Department of Otolaryngology-Head and Neck Surgery, Xiangya Hospital, Central South University, Changsha, PR China, Department of Otolaryngology (D-48), University of Miami Miller School of Medicine, Miami, FL, United States of America
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Lu Jiang
* E-mail: 44496635@QQ.com
Affiliations Department of Otolaryngology-Head and Neck Surgery, Xiangya Hospital, Central South University, Changsha, PR China, Key Laboratory of Otolaryngology Major Disease Research of Hunan Province, Changsha, PR China
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A novel frameshift mutation of SMPX causes a rare form of X-linked nonsyndromic hearing loss in a Chinese family
- Zhijie Niu,
- Yong Feng,
- Lingyun Mei,
- Jie Sun,
- Xueping Wang,
- Juncheng Wang,
- Zhengmao Hu,
- Yunpeng Dong,
- Hongsheng Chen,
- Chufeng He
- Published: May 25, 2017
- https://doi.org/10.1371/journal.pone.0178384