The variable phenotypes of KCNQ-related epilepsy

Author:

Allen Nicholas M.1,Mannion Maria1,Conroy Judith2,Lynch Sally A.23,Shahwan Amre1,Lynch Bryan1,King Mary D.12

Affiliation:

1. Department of Paediatric Neurology & Clinical Neurophysiology; Children's University Hospital; Dublin Ireland

2. Academic Centre on Rare Diseases; School of Medicine and Medical Science; University College; Dublin Ireland

3. Department of Clinical Genetics; Children's University Hospital; Temple St. Dublin Ireland

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference24 articles.

1. Genetic testing in benign familial epilepsies of the first year of life: clinical and diagnostic significance;Zara;Epilepsia,2013

2. Genetics of epilepsy syndromes starting in the first year of life;Deprez;Neurology,2009

3. Benign familial neonatal convulsions caused by mutation in KCNQ3, exon 6: a European case;Fister;Eur J Paediatr Neurol,2013

4. Contiguous deletion of KCNQ2 and CHRNA4 may cause a different disorder from benign familial neonatal seizures;Pascual;Epilepsy Behav Case Rep,2013

5. Benign familial neonatal convulsions: always benign?;Steinlein;Epilepsy Res,2007

Cited by 104 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