Identification and Functional Study of a New Missense Mutation in the Motor Head Domain of Myosin VIIA in a Family with Autosomal Dominant Hearing Impairment (DFNA11)

• Qing Sang ,

  Contributed equally to this work with: Qing Sang, Xukun Yan, Huan Wang

  Affiliations State Key Laboratory of Genetic Engineering and MOE Key Laboratory of Contemporary Anthropology, School of Life Sciences, Fudan University, Shanghai, People's Republic of China, Institutes of Biomedical Sciences, Fudan University, Shanghai, People's Republic of China

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• Xukun Yan ,

  Contributed equally to this work with: Qing Sang, Xukun Yan, Huan Wang

  Affiliations Department of Otolaryngology, Eye & ENT Hospital, Fudan University, Shanghai, People's Republic of China, Department of Otolaryngology, Chinese PLA General Hospital, Beijing, People's Republic of China

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• Huan Wang ,

  Contributed equally to this work with: Qing Sang, Xukun Yan, Huan Wang

  Affiliations State Key Laboratory of Genetic Engineering and MOE Key Laboratory of Contemporary Anthropology, School of Life Sciences, Fudan University, Shanghai, People's Republic of China, Institutes of Biomedical Sciences, Fudan University, Shanghai, People's Republic of China

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• Ruizhi Feng,

  Affiliations State Key Laboratory of Genetic Engineering and MOE Key Laboratory of Contemporary Anthropology, School of Life Sciences, Fudan University, Shanghai, People's Republic of China, Institutes of Biomedical Sciences, Fudan University, Shanghai, People's Republic of China

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• Xiang Fei,

  Affiliation Fudan-VARI Center for Genetic Epidemiology, Fudan University, Shanghai, People's Republic of China

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• Duan Ma,

  Affiliation Department of Otolaryngology, Eye & ENT Hospital, Fudan University, Shanghai, People's Republic of China

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• Qinghe Xing,

  Affiliations Institutes of Biomedical Sciences, Fudan University, Shanghai, People's Republic of China, Bio-X Center, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders, Ministry of Education, Shanghai Jiao Tong University, Shanghai, People's Republic of China

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• Qiaoli Li,

  Affiliations Institutes of Biomedical Sciences, Fudan University, Shanghai, People's Republic of China, Bio-X Center, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders, Ministry of Education, Shanghai Jiao Tong University, Shanghai, People's Republic of China

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• Xinzhi Zhao,

  Affiliations Institutes of Biomedical Sciences, Fudan University, Shanghai, People's Republic of China, Bio-X Center, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders, Ministry of Education, Shanghai Jiao Tong University, Shanghai, People's Republic of China

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• Li Jin,

  Affiliation State Key Laboratory of Genetic Engineering and MOE Key Laboratory of Contemporary Anthropology, School of Life Sciences, Fudan University, Shanghai, People's Republic of China

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• Lin He,

  Affiliations Institutes of Biomedical Sciences, Fudan University, Shanghai, People's Republic of China, Bio-X Center, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders, Ministry of Education, Shanghai Jiao Tong University, Shanghai, People's Republic of China

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• Huawei Li ,

  * E-mail: hwli@shmu.edu.cn (HWL); wangleiwanglei@fudan.edu.cn. (LW)

  Affiliation Department of Otolaryngology, Eye & ENT Hospital, Fudan University, Shanghai, People's Republic of China

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• Lei Wang

  * E-mail: hwli@shmu.edu.cn (HWL); wangleiwanglei@fudan.edu.cn. (LW)

  Affiliations State Key Laboratory of Genetic Engineering and MOE Key Laboratory of Contemporary Anthropology, School of Life Sciences, Fudan University, Shanghai, People's Republic of China, Institutes of Biomedical Sciences, Fudan University, Shanghai, People's Republic of China, Bio-X Center, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders, Ministry of Education, Shanghai Jiao Tong University, Shanghai, People's Republic of China

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