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

Informa Healthcare

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Molecular epidemiological analysis of mitochondrial DNA12SrRNA A1555G, GJB2, and SLC26A4 mutations in sporadic outpatients with nonsyndromic sensorineural hearing loss in China

By Ji Yu-bin   Han Dong-Yi   Lan Lan   Wang Da-Yong   Zong Liang   Zhao Fei-Fan   Liu Qiong   Benedict-Alderfer Cindy   Zheng Qing-yin   Wang Qiu-Ju  

Acta Oto-Laryngologica, Vol. 131, Iss. 2, 2011-02 ,pp. : 124-129

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Audiological profile of the prevalent genetic form of childhood sensorineural hearing loss due to GJB2 mutations in northern Greece

By Iliadou V.   Eleftheriades N.   Metaxas A.   Skevas A.   Kiratzidis T.   Pampanos A.   Voyiatzis N.   Grigoriadou M.   Petersen M.   Iliades T.  

European Archives of Oto-Rhino-Laryngology, Vol. 261, Iss. 5, 2004-05 ,pp. : 259-261

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

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

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Temporal Bone High-Resolution Computed Tomography in Non-Syndromic Unilateral Hearing Loss in Children

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ORL, Vol. 74, Iss. 2, 2012-02 ,pp. : 70-77

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