Potassium Channel Subunit Kir4.1 Mutated in Paroxysmal Kinesigenic Dyskinesia: Screening of an Italian Cohort-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Potassium Channel Subunit Kir4.1 Mutated in Paroxysmal Kinesigenic Dyskinesia: Screening of an Italian Cohort

Published:2024-08-29 Issue: Volume: Page:
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Movement Disorders

Author:

Zorzi Giovanna¹^ORCID,Zibordi Federica¹,Sorrentino Ugo²³⁴,Prokisch Holger²³,Garavaglia Barbara⁵,Zech Michael²³⁶^ORCID

Affiliation:

1. Unit of Child Neuropsychiatry–Movement Disorder Fondazione IRCCS Istituto Neurologico Carlo Besta Milan Italy

2. Institute of Human Genetics Technical University of Munich, School of Medicine and Health Munich Germany

3. Helmholtz Center Munich Institute of Neurogenomics Neuherberg Germany

4. Clinical Genetics Unit, Department of Women's and Children's Health University of Padova Padova Italy

5. Medical Genetics and Neurogenetics Unit Fondazione IRCCS Istituto Neurologico Carlo Besta Milan Italy

6. Institute for Advanced Study Technical University of Munich Garching Germany

Publisher

Wiley

Reference7 articles.

1. Rare Missense Variants in KCNJ10 Are Associated with Paroxysmal Kinesigenic Dyskinesia

2. Heterozygous Variants in KCNJ10 Cause Paroxysmal Kinesigenic Dyskinesia Via Haploinsufficiency

3. Potassium Channel KIR4.1 as an Immune Target in Multiple Sclerosis

4. Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in KCNJ10

5. Monogenic variants in dystonia: an exome-wide sequencing study

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