SCN1Amutations and epilepsy
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference67 articles.
1. Partial and generalized epilepsy with febrile seizures plus an a novel SCN1A mutation;Abou-Khalil;Neurology,2001
2. A sodium channel mutation causing epilepsy in man exhibits subtle defects in fast inactivation and activation in vitro;Alekov;J Physiol,2000
3. Two mutations in the IV/S4-S5 segment of the human skeletal muscle Na+ channel disrupt fast and enhance slow inactivation;Alekov;Neurosci Lett,2001
4. Two novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus;Annesi;Epilepsia,2003
5. Molecular mechanism for an inherited cardiac arrhythmia;Bennett;Nature,1995
Cited by 303 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Voltage-gated sodium channel epilepsies in a tertiary care center: Phenotypic spectrum with correlation to predicted functional effects;Epilepsy & Behavior;2024-09
2. The Role of Glutamate and Blood–Brain Barrier Disruption as a Mechanistic Link between Epilepsy and Depression;Cells;2024-07-21
3. A high seizure burden increases several prostaglandin species in the hippocampus of a Scn1a mouse model of Dravet syndrome;Prostaglandins & Other Lipid Mediators;2024-06
4. In vitro human cell culture models in a bench‐to‐bedside approach to epilepsy;Epilepsia Open;2024-04-18
5. Meta-analysis of 46,000 germline de novo mutations linked to human inherited disease;Human Genomics;2024-02-23
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3