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Acta Oto-Laryngologica Volume 136, 2016 - Issue 8
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Research Article

GJB2, SLC26A4, and mitochondrial DNA12S rRNA hot-spots in 156 subjects with non-syndromic hearing loss in Tengzhou, China

Yalin MaDepartment of Otorhinolaryngology Head and Neck Surgery, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, PR China; ;Shandong Provincial Key Laboratory of Otology, Jinan, PR China; ;Department of Otorhinolaryngology Head and Neck Surgery, Tengzhou Central People’s Hospital, Shandong, PR China
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Yun XiaoDepartment of Otorhinolaryngology Head and Neck Surgery, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, PR China; ;Shandong Provincial Key Laboratory of Otology, Jinan, PR China;
,
Xiaohui BaiDepartment of Otorhinolaryngology Head and Neck Surgery, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, PR China; ;Shandong Provincial Key Laboratory of Otology, Jinan, PR China;
,
Fengguo ZhangDepartment of Otorhinolaryngology Head and Neck Surgery, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, PR China; ;Shandong Provincial Key Laboratory of Otology, Jinan, PR China;
,
Daogong ZhangDepartment of Otorhinolaryngology Head and Neck Surgery, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, PR China; ;Shandong Provincial Key Laboratory of Otology, Jinan, PR China;
,
Xinmao XuDepartment of Otorhinolaryngology Head and Neck Surgery, Tengzhou Central People’s Hospital, Shandong, PR China
,
Lei XuDepartment of Otorhinolaryngology Head and Neck Surgery, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, PR China; ;Shandong Provincial Key Laboratory of Otology, Jinan, PR China;
&
Haibo WangDepartment of Otorhinolaryngology Head and Neck Surgery, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, PR China; ;Shandong Provincial Key Laboratory of Otology, Jinan, PR China; Correspondence[email protected]
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Pages 800-805 | Received 15 Jan 2016, Accepted 29 Feb 2016, Published online: 12 Apr 2016

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Meng Zhang, Yuechen Han, Fengguo Zhang, Xiaohui Bai & Haibo Wang. (2019) Mutation spectrum and hotspots of the common deafness genes in 314 patients with nonsyndromic hearing loss in Heze area, China. Acta Oto-Laryngologica 139:7, pages 612-617.
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Articles from other publishers (11)

Nandita Sharma, Divya Kumari, Inusha Panigrahi & Preeti Khetarpal. (2022) A systematic review of the monogenic causes of Non‐Syndromic Hearing Loss (NSHL) and discussion of Current Diagnosis and Treatment options. Clinical Genetics 103:1, pages 16-34.
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Yasunori Maeda, Akira Sasaki, Shuya Kasai, Shinichi Goto, Shin-ya Nishio, Kaori Sawada, Itoyo Tokuda, Ken Itoh, Shin-ichi Usami & Atsushi Matsubara. (2020) Prevalence of the mitochondrial 1555 A>G and 1494 C>T mutations in a community-dwelling population in Japan. Human Genome Variation 7:1.
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Yongan Zhou, Chao Li, Min Li, Zhonghua Zhao, Shuxiong Tian, Hou Xia, Peixian Liu, Yaxin Han, Ruirui Ren, Jianping Chen, Caihong Jia & Wei Guo. (2019) Mutation analysis of common deafness genes among 1,201 patients with non‐syndromic hearing loss in Shanxi Province. Molecular Genetics & Genomic Medicine 7:3.
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Jae Joon Han, Pham Dinh Nguyen, Doo-Yi Oh, Jin Hee Han, Ah-Reum Kim, Min Young Kim, Hye-Rim Park, Lam Huyen Tran, Nguyen Huu Dung, Ja-Won Koo, Jun Ho Lee, Seung Ha Oh, Hoang Anh Vu & Byung Yoon Choi. (2019) Elucidation of the unique mutation spectrum of severe hearing loss in a Vietnamese pediatric population. Scientific Reports 9:1.
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Pingsen Zhao, Lifang Lin & Liubing Lan. (2018) Analysis of mutation spectrum of common deafness-causing genes in Hakka newborns in southern China by semiconductor sequencing. Medicine 97:38, pages e12285.
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Bangqing Huang, Mingyu Han, Guojian Wang, ShaSha Huang, Jialing Zeng, Yongyi Yuan & Pu Dai. (2018) Genetic mutations in non-syndromic deafness patients in Hainan Province have a different mutational spectrum compared to patients from Mainland China. International Journal of Pediatric Otorhinolaryngology 108, pages 49-54.
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Fengguo Zhang, Lei Xu, Yun Xiao, Jianfeng Li, Xiaohui Bai & Haibo Wang. (2018) Three MYO15A Mutations Identified in One Chinese Family with Autosomal Recessive Nonsyndromic Hearing Loss . Neural Plasticity 2018, pages 1-8.
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Y Ding, B-H Xia, Y-S Teng, G-C Zhuo & J-H Leng. (2017) The mitochondrial COI/tRNA SER(UCN) G7444A mutation may be associated with hearing impairment in a Han Chinese family . Balkan Journal of Medical Genetics 20:2, pages 43-49.
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Xinyi Zhang, Bo LiangXiaoyan Xu, Feifei Zhou, Lingyin Kong, Jingjing Shen, Yingying Xia, Liming Xuan, Yan Mao, Yongfeng Xue, Caixia LiuJichun Tan. (2017) The comparison of the performance of four whole genome amplification kits on ion proton platform in copy number variation detection. Bioscience Reports 37:4.
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Siping Li, Qi Peng, Shengyun Liao, Wenrui Li, Qiang Ma & Xiaomei Lu. (2017) A reverse dot blot assay for the screening of twenty mutations in four genes associated with NSHL in a Chinese population. PLOS ONE 12:5, pages e0177196.
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Chi Zhang, Mingming Wang, Yun Xiao, Fengguo Zhang, Yicui Zhou, Jianfeng Li, Qingyin Zheng, Xiaohui Bai & Haibo Wang. (2016) A Novel Nonsense Mutation of POU4F3 Gene Causes Autosomal Dominant Hearing Loss . Neural Plasticity 2016, pages 1-10.
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