CORC

浏览/检索结果: 共7条,第1-7条 帮助

限定条件    
已选(0)清除 条数/页:   排序方式:
CRB2 mutation causes autosomal recessive retinitis pigmentosa 期刊论文
EXPERIMENTAL EYE RESEARCH, 2019, 卷号: 180
作者:  Sun, Ruxu;  Chen, Xue;  Jiang, Chao;  Yang, Daidi;  Wang, Min
收藏  |  浏览/下载:22/0  |  提交时间:2019/12/05
Whole-exome sequencing identifies novel mutations in genes responsible for retinitis pigmentosa in 2 nonconsanguineous Chinese families 期刊论文
INTERNATIONAL JOURNAL OF OPHTHALMOLOGY, 2019, 卷号: 12, 期号: 6
作者:  Hu, Yan-Shan;  Song, Hui;  Li, Yin;  Xiao, Zi-Yun;  Li, Tuo
收藏  |  浏览/下载:3/0  |  提交时间:2019/12/05
A Novel CNGA1 Gene Mutation (c.G622A) of Autosomal Recessive Retinitis Pigmentosa Leads to the CNGA1 Protein Reduction on Membrane 期刊论文
BIOCHEMICAL GENETICS, 2019, 卷号: 57, 期号: 4
作者:  Gao, Qing;  Liu, Yifan;  Lei, Xinlan;  Deng, Qinqin;  Tong, Yongqing
收藏  |  浏览/下载:10/0  |  提交时间:2019/12/05
Vitamins and Mineral Supplements for Retinitis Pigmentosa 期刊论文
2019
作者:  Zhao, Ying[1];  Feng, Kai[2];  Liu, Ruibao[1];  Pan, Jinhua[1];  Zhang, Lailin[1]
收藏  |  浏览/下载:28/0  |  提交时间:2019/12/06
Altered intra- and inter-regional functional connectivity of the visual cortex in individuals with peripheral vision loss due to retinitis pigmentosa 期刊论文
VISION RESEARCH, 2019, 卷号: 159
作者:  Dan, Han-Dong;  Zhou, Fu-Qing;  Huang, Xin;  Xing, Yi-Qiao;  Shen, Yin
收藏  |  浏览/下载:11/0  |  提交时间:2019/12/05
Abnormal intrinsic functional network hubs and connectivity following peripheral visual loss because of inherited retinal degeneration 期刊论文
NEUROREPORT, 2019, 卷号: 30, 期号: 4
作者:  Huang, Xin;  Dan, Han-Dong;  Zhou, Fu-Qing;  Deng, Qin-Qin;  Shen, Yin
收藏  |  浏览/下载:9/0  |  提交时间:2019/12/05
Genetic and Clinical Findings in a Large Cohort of Chinese Patients with Suspected Retinitis Pigmentosa 期刊论文
2019
作者:  Gao Feng-Juan;  Li Jian-Kang;  Chen Han;  Hu Fang-Yuan;  Zhang Sheng-Hai
收藏  |  浏览/下载:21/0  |  提交时间:2020/01/03


©版权所有 ©2017 CSpace - Powered by CSpace