Three common GJB2 mutations causing nonsyndromic hearing loss in Chinese populations are retained in the endoplasmic reticulum

By Zhang Yanping   Wang Ju   Li Lina   Sun Yurui   Feng Bo  

Acta Oto-Laryngologica, Vol. 130, Iss. 7, 2010-07 ,pp. : 799-803

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An Analysis of a Large Postlingually Deaf Family with Hereditary Non-syndromic Profound Hearing Loss

By Angeli Simón I.   Naranjo Carlos   Friedman Rick A.   Naranjo Alfredo   Henríquez Oswaldo   Fischel-Ghodsian Nathan   Chiossone Edgar  

Acta Oto-Laryngologica, Vol. 119, Iss. 2, 1999-04 ,pp. : 158-162

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Novel mutations of SLC26A4 in Chinese patients with nonsyndromic hearing loss

By Yao Gendong   Chen Dingli   Wang Huijun   Li Shouxia   Zhang Jin   Feng Zhixing   Guo Lili   Yang Zhiming   Yang Sujun   Sun Caixia   Zhang Xiaofang   Ma Duan  

Acta Oto-Laryngologica, Vol. 133, Iss. 8, 2013-08 ,pp. : 833-841

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Low prevalence of GJB2 mutations in non-syndromic hearing loss in Western India

By Godbole Koumudi  

Indian Journal of Otolaryngology, Vol. 62, Iss. 1, 2010-01 ,pp. : 60-63

Springer Publishing Company

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Common molecular etiology of patients with nonsyndromic hearing loss in Tibetan, Tu nationality, and Mongolian patients in the northwest of China

By Yang Xiao-Long   Bai-Cheng Xu   Chen Xing-Jian   Pan-Pan Bian   Jian-Li Ma   Xiao-Wen Liu   Zhang Zhe-Wen   Wan Du   Zhu Yi-Ming   Guo Yu-Fen  

Acta Oto-Laryngologica, Vol. 133, Iss. 9, 2013-09 ,pp. : 930-934

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