Genes and loci involved in febrile seizures and related epilepsy syndromes
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference69 articles.
1. Partial and generalized epilepsy with febrile seizures plus and a novel SCN1A mutation
2. Two Novel SCN1A Missense Mutations in Generalized Epilepsy with Febrile Seizures Plus
3. A deletion in SCN1B is associated with febrile seizures and early-onset absence epilepsy
4. A novel susceptibility locus at 2p24 for generalised epilepsy with febrile seizures plus
5. A Second Locus for Familial Generalized Epilepsy with Febrile Seizures Plus Maps to Chromosome 2q21-q33
Cited by 51 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. Seizures in Children with Influenza during the 2022–2023 Winter Season, a Case Series;Clinics and Practice;2024-01-19
2. Unlocking the link between haptoglobin polymorphism and noninfectious human diseases: insights and implications;Critical Reviews in Clinical Laboratory Sciences;2023-11-27
3. Molecular analysis and prenatal diagnosis of seven Chinese families with genetic epilepsy;Frontiers in Neuroscience;2023-05-12
4. Ion channels and febrile seizures: It’s not just SCN1A;Febrile Seizures;2023
5. CELSR3 variants are associated with febrile seizures and epilepsy with antecedent febrile seizures;CNS Neuroscience & Therapeutics;2021-12-23
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