Loss-of-Function Mutations in the PRPS1 Gene Cause a Type of Nonsyndromic X-linked Sensorineural Deafness, DFN2

Por Liu, Xuezhong, Han, Dongyi, Li, Jianzhong, Han, Bing, Ouyang, Xiaomei, Cheng, Jing, Li, Xu, Jin, Zhanguo, Wang, Youqin, Bitner-Glindzicz, Maria, Kong, Xiangyin, Xu, Heng, Kantardzhieva, Albena, Eavey, Roland D., Seidman, Christine E., Seidman, Jonathan G., Du, Li L., Chen, Zheng-Yi, Dai, Pu, Teng, Maikun, Yan, Denise, Yuan, Huijun
Publicado em 2010

GJB2 mutation spectrum in 2063 Chinese patients with nonsyndromic hearing impairment

Por Dai, Pu, Yu, Fei, Han, Bing, Liu, Xuezhong, Wang, Guojian, Li, Qi, Yuan, Yongyi, Liu, Xin, Huang, Deliang, Kang, Dongyang, Zhang, Xin, Yuan, Huijun, Yao, Kun, Hao, Jinsheng, He, Jia, He, Yong, Wang, Youqin, Ye, Qing, Yu, Youjun, Lin, Hongyan, Liu, Lijia, Deng, Wei, Zhu, Xiuhui, You, Yiwen, Cui, Jinghong, Hou, Nongsheng, Xu, Xuehai, Zhang, Jin, Tang, Liang, Song, Rendong, Lin, Yongjun, Sun, Shuanzhu, Zhang, Ruining, Wu, Hao, Ma, Yuebing, Zhu, Shanxiang, Wu, Bai-lin, Han, Dongyi, Wong, Lee-Jun C
Publicado em 2009