A novelKCNQ3mutation in familial epilepsy with focal seizures and intellectual disability

Author:

Miceli Francesco1,Striano Pasquale2ORCID,Soldovieri Maria Virginia3,Fontana Antonina4,Nardello Rosaria4,Robbiano Angela5,Bellini Giulia6,Elia Maurizio7,Zara Federico5,Taglialatela Maurizio138,Mangano Salvatore4

Affiliation:

1. Unit of Pharmacology; Department of Neuroscience; Reproductive Science and Dentistry; University of Naples Federico II; Naples Italy

2. Unit of Pediatric Neurology and Muscular Diseases; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health; University of Genoa; “G. Gaslini” Institute; Genova Italy

3. Department of Medicine and Health Science; University of Molise; Campobasso Italy

4. Unit of Child Neuropsychiatry; Department of Sciences for Health Promotion and Mother and Child Care “G. D'Alessandro,”; University of Palermo; Palermo Italy

5. Laboratory of Neurogenetics; Department of Neuroscience; “G. Gaslini” Institute; Genoa Italy

6. Department of Pediatrics; Second University of Naples; Naples Italy

7. IRCCS “Oasi Maria SS”; Troina (EN) Italy

8. Units of Biophysics, National Research Council of Spain; University of the Basque Country; Leioa Spain

Publisher

Wiley

Subject

Clinical Neurology,Neurology

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