The prevalence of LRRK2 Gly2385Arg variant in Chinese Han population with Parkinson's disease
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Reference20 articles.
1. Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease;Paisan-Ruiz;Neuron,2004
2. Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology;Zimprich;Neuron,2004
3. Parkinson's disease due to the R1441G mutation in Dardarin: a founder effect in the Basques;Simon-Sanchez;Mov Disord,2006
4. LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews;Ozelius;N Engl J Med,2006
5. LRRK2 G2019S in families with Parkinson disease who originated from Europe and the Middle East: evidence of two distinct founding events beginning two millennia ago;Zabetian;Am J Hum Genet,2006
Cited by 48 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. Clinical and genetic analysis of Vietnamese patients diagnosed with early‐onset Parkinson's disease;Brain and Behavior;2023-03-06
2. Genetic variations in GBA1 and LRRK2 genes: Biochemical and clinical consequences in Parkinson disease;Frontiers in Neurology;2022-08-12
3. Connectivity of corticostriatal circuits in nonmanifesting LRRK2 G2385R and R1628P carriers;CNS Neuroscience & Therapeutics;2022-08-07
4. Pathophysiological evaluation of the LRRK2 G2385R risk variant for Parkinson’s disease;npj Parkinson's Disease;2022-08-05
5. Leucine-rich repeat kinase 2 (LRRK2): an update on the potential therapeutic target for Parkinson’s disease;Expert Opinion on Therapeutic Targets;2022-06-02
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