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Association of the hERG mutation with long-QT syndrome type 2, syncope and epilepsy 期刊论文
MOLECULAR MEDICINE REPORTS, 2016, 卷号: 13, 期号: [db:dc_citation_issue], 页码: 2467-2475
作者:  Li, Guoliang;  Shi, Rui;  Wu, Jine;  Han, Wenqi;  Zhang, Aifeng
收藏  |  浏览/下载:3/0  |  提交时间:2019/12/02
Clinical features of Dravet syndrome patients with SCN1A gene mutations 期刊论文
Journal of Xi'an Jiaotong University (Medical Sciences), 2016, 卷号: 37, 页码: 841-845
作者:  Li, Dan;  Huang, Shao-Ping;  Song, Ting-Ting;  Yang, Lin;  Yang, Chang-Hong
收藏  |  浏览/下载:8/0  |  提交时间:2019/11/26
A POTENT DOMINANT NEGATIVE MUTATION IN HERG IN A CHINESE FAMILY EXPERIENCING LONG QT SYNDROME, EPILEPSY, AND UNEXPECTED SUDDEN DEATH 期刊论文
CARDIOLOGY, 2014, 卷号: 128, 期号: [db:dc_citation_issue], 页码: 84-84
作者:  Li, G. L.;  Wu, J. E.;  Han, W. Q.;  Ma, S. T.;  Zhang, A. F.
收藏  |  浏览/下载:3/0  |  提交时间:2019/12/02
Hyper IgE syndrome. 期刊论文
Indian dermatology online journal, 2014, 卷号: 5, 期号: [db:dc_citation_issue], 页码: 69-71
作者:  Dang Yun;  Ren Jianwen;  Guo Yuanyuan;  Geng Songmei
收藏  |  浏览/下载:3/0  |  提交时间:2019/12/02
Hyper-IgE syndrome with rare associations of epilepsy: A case report 期刊论文
JOURNAL OF DERMATOLOGY, 2012, 卷号: 39, 期号: [db:dc_citation_issue], 页码: 180-180
作者:  Dang Yun;  Ren Jian-wen;  Guo Yuan-yuan;  Geng Song-mei
收藏  |  浏览/下载:1/0  |  提交时间:2019/12/10


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