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Co-Existence of Novel PDE6A Mutations and A Recurrent RPGR Mutation: A Potential Explanation for Phenotypic Diversity in Female RPGR Mutation Carriers 期刊论文
CURRENT MOLECULAR MEDICINE, 2018, 卷号: 18, 期号: 5
作者:  Chen, X.;  Sheng, X.;  Liu, G.;  Liu, Y.;  Li, H.
收藏  |  浏览/下载:7/0  |  提交时间:2019/12/05
Co-Existence of Novel PDE6A Mutations and A Recurrent RPGR Mutation: A Potential Explanation for Phenotypic Diversity in Female RPGR Mutation Carriers 期刊论文
CURRENT MOLECULAR MEDICINE, 2018, 卷号: 18, 期号: 5, 页码: 306-311
作者:  Chen, X.;  Sheng, X.;  Liu, G.;  Liu, Y.;  Li, H.
收藏  |  浏览/下载:3/0  |  提交时间:2019/12/11
A heterozygous mutation in RPGR associated with X-linked retinitis pigmentosa in a patient with Turner syndrome mosaicism (45,X/46,XX) 期刊论文
2018, 卷号: 176, 期号: 1, 页码: 214-218
作者:  Zhou, Qi;  Yao, Fengxia;  Wang, Feng;  Li, Hui;  Chen, Rui
收藏  |  浏览/下载:7/0  |  提交时间:2020/01/03
Novel RPGR-ORF15 mutations in X-linked retinitis pigmentosa patients 期刊论文
NEUROSCIENCE LETTERS, 2011, 卷号: 500, 期号: 1
作者:  Gan, De-Kang;  He, Chen-Liang;  Shu, Hai-Rong;  Hoffman, Matthew R.;  Jin, Zi-Bing
收藏  |  浏览/下载:2/0  |  提交时间:2019/12/19


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