A subset of genomic alterations detected in rolandic epilepsies contains candidate or known epilepsy genes includingGRIN2AandPRRT2

Author:

Dimassi Sarra123,Labalme Audrey14,Lesca Gaetan1234,Rudolf Gabrielle456,Bruneau Nadine4789,Hirsch Edouard45,Arzimanoglou Alexis3410,Motte Jacques411,de Saint Martin Anne412,Boutry-Kryza Nadia23413,Cloarec Robin4789,Benitto Afaf11,Ameil Agnès11,Edery Patrick123,Ryvlin Philippe23414,De Bellescize Julitta410,Szepetowski Pierre4789,Sanlaville Damien1234

Affiliation:

1. Department of Genetics; Lyon University Hospital; Lyon France

2. Claude Bernard Lyon I University; Lyon France

3. CRNL; CNRS UMR 5292; INSERM U1028; Lyon France

4. The French EPILAND (Epilepsy, Language and Development) Consortium; Marseille France

5. Department of Neurology; Strasbourg University Hospital; Strasbourg France

6. UMR_S; INSERM U1119; Strasbourg France

7. INSERM Unit U901; Marseille France

8. Mediterranean Institute of Neurobiology (INMED); Marseille France

9. UMR_S901; Aix-Marseille University; Marseille France

10. Departments of Epilepsy, Sleep and Pediatric Neurophysiology (ESEFNP); University Hospitals of Lyon (HCL); Lyon France

11. Department of Pediatry A; American Memorial Hospital; Reims University Hospital; Reims France

12. Department of Pediatry I; Strasbourg University Hospital; Strasbourg France

13. Department of Molecular Genetics; Lyon University Hospital; Lyon France

14. Department of Neurology; Lyon University Hospital; Lyon France

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Cited by 73 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

同舟云学术

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