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A knock-in mouse model of Pendred syndrome with Slc26a4 L236P mutation 期刊论文
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2019, 卷号: 515, 期号: 2, 页码: 359-365
作者:  Wen, Zongzhuang;  Zhu, Haixia;  Li, Zhenzu;  Zhang, Sen;  Zhang, Aizhen
收藏  |  浏览/下载:4/0  |  提交时间:2019/12/11
Construction of a multiplex allele-specific PCR-based universal array (ASPUA) and its application to hearing loss screening 期刊论文
2010, 2010
Li, Cai-Xia; Pan, Qian; Guo, YongGang; Li, Yan; Gao, Hua-Fang; Zhang, Di; Hu, Hao; Xing, Wan Li; Mitchelson, Keith; Xia, Kun; Dai, Pu; Cheng, Jing
收藏  |  浏览/下载:7/0
An association study of the slc26a4 gene in children with mental retardation 期刊论文
Neuroscience letters, 2009, 卷号: 457, 期号: 3, 页码: 155-158
作者:  Li, Jun;  Zhang, Fuchang;  Gao, Jianjun;  Cai, Zhen;  Zhao, Qian
收藏  |  浏览/下载:23/0  |  提交时间:2019/05/10
Distinct and novel SLC26A4/Pendrin mutations in Chinese and US patients with nonsyndromic hearing loss 期刊论文
PHYSIOLOGICAL GENOMICS, 2009, 卷号: 38, 期号: 3
作者:  Dai, Pu;  Stewart, Andrew K.;  Chebib, Fouad;  Hsu, Ann;  Rozenfeld, Julia
收藏  |  浏览/下载:10/0  |  提交时间:2019/12/19


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