<it>GJB2 </it>mutation spectrum in 2063 Chinese patients with nonsyndromic hearing impairment

<it>GJB2 </it>mutation spectrum in 2063 Chinese patients with nonsyndromic hearing impairment

<p>Abstract</p> <p>Background</p> <p>Mutations in <it>GJB2 </it>are the most common molecular defects responsible for autosomal recessive nonsyndromic hearing impairment (NSHI). The mutation spectra of this gene vary among different ethnic groups.</p>...

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Main Authors: Tang Liang, Zhang Jin, Xu Xuehai, Hou Nongsheng, Cui Jinghong, You Yiwen, Zhu Xiuhui, Deng Wei, Liu Lijia, Lin Hongyan, Yu Youjun, Ye Qing, Wang Youqin, He Yong, He Jia, Hao Jinsheng, Yao Kun, Yuan Huijun, Zhang Xin, Kang Dongyang, Huang Deliang, Liu Xin, Yuan Yongyi, Li Qi, Wang Guojian, Liu Xuezhong, Han Bing, Yu Fei, Dai Pu, Song Rendong, Lin Yongjun, Sun Shuanzhu, Zhang Ruining, Wu Hao, Ma Yuebing, Zhu Shanxiang, Wu Bai-lin, Han Dongyi, Wong Lee-Jun C
Format: Article
Language:English
Published: BMC 2009-04-01
Series:Journal of Translational Medicine
Online Access:http://www.translational-medicine.com/content/7/1/26

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