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Whole-exome sequencing revealed HKDC1 as a candidate gene associated with autosomal-recessive retinitis pigmentosa 期刊论文
2018, 卷号: 27, 期号: 23, 页码: 4157-4168
作者:  Zhang, Lin;  Sun, Zixi;  Zhao, Peiquan;  Huang, Lulin;  Xu, Mingchu
收藏  |  浏览/下载:7/0  |  提交时间:2020/01/03
CEP78 is mutated in a distinct type of Usher syndrome 期刊论文
2017, 卷号: 54, 期号: 3, 页码: 190-195
作者:  Fu, Qing;  Xu, Mingchu;  Chen, Xue;  Sheng, Xunlun;  Yuan, Zhisheng
收藏  |  浏览/下载:4/0  |  提交时间:2020/01/04
IFT81 as a Candidate Gene for Nonsyndromic Retinal Degeneration 期刊论文
2017, 卷号: 58, 期号: 5, 页码: 3483-3490
作者:  Dharmat Rachayata;  Liu Wei;  Ge Zhongqi;  Sun Zixi;  Yang Lizhu
收藏  |  浏览/下载:2/0  |  提交时间:2020/01/04
Mutations in POMGNT1 cause non-syndromic retinitis pigmentosa 期刊论文
2016, 卷号: 25, 期号: 8, 页码: 1479-1488
作者:  Xu, Mingchu;  Yamada, Takeyuki;  Sun, Zixi;  Eblimit, Aiden;  Lopez, Irma
收藏  |  浏览/下载:5/0  |  提交时间:2020/01/04
Investigation of drugs responsible for perioperative anaphylactic reactions using cellular allergen stimulation test 期刊论文
2014, 卷号: 127, 期号: 21, 页码: 3738-3743
作者:  Xin Xin;  Zou Yi;  Xing Lijiao;  Yin Jia;  Gu Jianqing
收藏  |  浏览/下载:5/0  |  提交时间:2020/01/13


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