QQ客服 官方微博 反馈留言

	Association between SCN1A and SCN2A mutations and clinical/EEG features in Chinese patients from epilepsy or severe seizures
	Kong, Yanting; Yan, Kai; Hu, Liyuan; Wang, Mingbang; Dong, Xinran; Lu, Yulan; Wu, Bingbing; Wang, Huijun; Yang, Lin; Zhou, Wenhao
刊名	CLINICA CHIMICA ACTA
	2018
卷号	483
关键词	SCN1A SCN2A Epilepsy Genotype Phenotype
ISSN号	0009-8981
URL标识	查看原文
语种	英语
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/3608825
专题	复旦大学上海医学院
推荐引用方式 GB/T 7714	Kong, Yanting,Yan, Kai,Hu, Liyuan,et al. Association between SCN1A and SCN2A mutations and clinical/EEG features in Chinese patients from epilepsy or severe seizures[J]. CLINICA CHIMICA ACTA,2018,483.
APA	Kong, Yanting.,Yan, Kai.,Hu, Liyuan.,Wang, Mingbang.,Dong, Xinran.,...&Zhou, Wenhao.(2018).Association between SCN1A and SCN2A mutations and clinical/EEG features in Chinese patients from epilepsy or severe seizures.CLINICA CHIMICA ACTA,483.
MLA	Kong, Yanting,et al."Association between SCN1A and SCN2A mutations and clinical/EEG features in Chinese patients from epilepsy or severe seizures".CLINICA CHIMICA ACTA 483(2018).

个性服务

查看访问统计

相关权益政策

暂无数据

收藏/分享

除非特别说明，本系统中所有内容都受版权保护，并保留所有权利。