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). |
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