[Investigation of clinical features and detection of 79 known deafness genes in a large Chinese family with dominant non-syndromic hearing loss].

Lin, Xiaojiang; Chen, Dongye; Wu, Hao; Yang, Tao; Zhang, Dan; Chai, Yongchuan

Lin, Xiaojiang; Chen, Dongye; Wu, Hao; Yang, Tao; Zhang, Dan; Chai, Yongchuan.

Afiliación

Lin X; Department of Otorhinolaryngology, People's Hospital of Kaihua, Zhejiang 324300, China.
Wu H; Department of Otolaryngology Head and Neck Surgery,Xinhua Hospital, Shanghai Jiaotong University School of Medicine, Shanghai Jiaotong University Ear Institute, Shanghai 200092, China. Email: wuhao622@sina.cn.

Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi ; 49(8): 654-8, 2014 Aug.

Article en Zh | MEDLINE | ID: mdl-25351123

Asunto(s)

Pérdida Auditiva/genética; Pueblo Asiatico; China; Conexina 26; Conexinas; Sordera; Pérdida Auditiva Sensorineural; Humanos; Mutación

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Bases de datos: MEDLINE Asunto principal: Pérdida Auditiva Tipo de estudio: Diagnostic_studies Límite: Humans País/Región como asunto: Asia Idioma: Zh Revista: Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi Año: 2014 Tipo del documento: Article País de afiliación: China

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