IR@PKUHSC  > 北京大学第一临床医学院
学科主题临床医学
APPROXIMATELY 10% OF "DE NOVO" SCN1AMUTATIONS CAUSING DRAVET SYNDROME ARE INHERITED FROM UNDETECTED PARENTAL MOSAICISM
Zhang, Y-H.1; Xu, X.1; Yang, X.2; Wu, Q.2; Wu, X.1; Wei, L.2
刊名EPILEPSIA
2015-02-01
suppl.1期:SI页:19-20
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:000365756500050
Citation statistics
文献类型期刊论文
条目标识符http://ir.bjmu.edu.cn/handle/400002259/67130
Collection北京大学第一临床医学院
作者单位1.Peking Univ, Hosp 1, Pediat, Beijing 100871, Peoples R China
2.Peking Univ, Sch Life Sci, Ctr Bioinformat, Beijing 100871, Peoples R China
Recommended Citation
GB/T 7714
Zhang, Y-H.,Xu, X.,Yang, X.,et al. APPROXIMATELY 10% OF "DE NOVO" SCN1AMUTATIONS CAUSING DRAVET SYNDROME ARE INHERITED FROM UNDETECTED PARENTAL MOSAICISM[J]. EPILEPSIA,2015,suppl.1(SI):19-20.
APA Zhang, Y-H.,Xu, X.,Yang, X.,Wu, Q.,Wu, X.,&Wei, L..(2015).APPROXIMATELY 10% OF "DE NOVO" SCN1AMUTATIONS CAUSING DRAVET SYNDROME ARE INHERITED FROM UNDETECTED PARENTAL MOSAICISM.EPILEPSIA,suppl.1(SI),19-20.
MLA Zhang, Y-H.,et al."APPROXIMATELY 10% OF "DE NOVO" SCN1AMUTATIONS CAUSING DRAVET SYNDROME ARE INHERITED FROM UNDETECTED PARENTAL MOSAICISM".EPILEPSIA suppl.1.SI(2015):19-20.
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