IR@PKUHSC  > 北京大学第一临床医学院  > 儿科
学科主题临床医学
ANALYSIS OF PRRT2 MUTATIONS IN CHINESE FAMILIES WITH BENIGN FAMILIAL INFANTILE EPILEPSY AND INFANTILE CONVULSIONS WITH PAROXYSMAL CHOREOATHETOSIS
Zhang, Y. H.; Yang, X. L.; Xu, X. J.; Wang, S.; Liu, X. Y.; Wu, Y.; Yang, Z. X.; Wu, X. R.
刊名EPILEPSIA
2013-06-01
suppl.3期:SI页:197-197
收录类别SCI ; ISTP
文章类型Meeting Abstract
WOS标题词Science & Technology
类目[WOS]Clinical Neurology
研究领域[WOS]Neurosciences & Neurology
语种英语
WOS记录号WOS:000320472000624
Citation statistics
文献类型期刊论文
条目标识符http://ir.bjmu.edu.cn/handle/400002259/63839
Collection北京大学第一临床医学院_儿科
作者单位Peking Univ, Dept Pediat, Hosp 1, Beijing 100871, Peoples R China
Recommended Citation
GB/T 7714
Zhang, Y. H.,Yang, X. L.,Xu, X. J.,et al. ANALYSIS OF PRRT2 MUTATIONS IN CHINESE FAMILIES WITH BENIGN FAMILIAL INFANTILE EPILEPSY AND INFANTILE CONVULSIONS WITH PAROXYSMAL CHOREOATHETOSIS[J]. EPILEPSIA,2013,suppl.3(SI):197-197.
APA Zhang, Y. H..,Yang, X. L..,Xu, X. J..,Wang, S..,Liu, X. Y..,...&Wu, X. R..(2013).ANALYSIS OF PRRT2 MUTATIONS IN CHINESE FAMILIES WITH BENIGN FAMILIAL INFANTILE EPILEPSY AND INFANTILE CONVULSIONS WITH PAROXYSMAL CHOREOATHETOSIS.EPILEPSIA,suppl.3(SI),197-197.
MLA Zhang, Y. H.,et al."ANALYSIS OF PRRT2 MUTATIONS IN CHINESE FAMILIES WITH BENIGN FAMILIAL INFANTILE EPILEPSY AND INFANTILE CONVULSIONS WITH PAROXYSMAL CHOREOATHETOSIS".EPILEPSIA suppl.3.SI(2013):197-197.
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