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Congenital disorder of glycosylation type 1T with a novel truncated homozygous mutation in PGM1 gene and literature review. 期刊论文
Neuromuscular disorders : NMD, 2019, 卷号: 29, 期号: 4
作者:  Tian Wo-Tu;  Luan Xing-Hua;  Zhou Hai-Yan;  Zhang Chao;  Huang Xiao-Jun
收藏  |  浏览/下载:4/0  |  提交时间:2019/12/06
The study of exercise tests in paroxysmal kinesigenic dyskinesia. 期刊论文
Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology, 2018, 卷号: 129, 期号: 11
作者:  Zhou Hai-Yan;  Zhan Fei-Xia;  Tian Wo-Tu;  Zhang Chao;  Wang Yan
收藏  |  浏览/下载:14/0  |  提交时间:2019/12/06
Progressive myoclonus epilepsy without renal failure in a Chinese family with a novel mutation in SCARB2 gene and literature 期刊论文
SEIZURE-EUROPEAN JOURNAL OF EPILEPSY, 2018, 卷号: 57
作者:  Tian, Wo-Tu;  Liu, Xiao-Li;  Xu, Yang-Qi;  Huang, Xiao-Jun;  Zhou, Hai-Yan
收藏  |  浏览/下载:4/0  |  提交时间:2019/12/06


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