Association study of rs6812193 polymorphism with Parkinson's disease in a Greek population
Author:
Publisher
Elsevier BV
Subject
General Neuroscience
Reference21 articles.
1. Array-based gene discovery with three unrelated subjects shows SCARB2/LIMP-2 deficiency causes myoclonus epilepsy and glomerulosclerosis;Berkovic;Am. J. Hum. Genet.,2008
2. Association study of SCARB2 rs6812193 polymorphism with Parkinson's disease in Han Chinese;Chen;Neurosci. Lett.,2012
3. Association of mutations in the glucocerebrosidase gene with Parkinson disease in a Korean population;Choi;Neurosci. Lett.,2012
4. Glucocerebrosidase gene mutations are associated with Parkinson's disease in southern Italy;De Marco;Mov. Disord.,2008
5. Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease;Do;PLoS Genet.,2011
Cited by 6 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. The Endo-lysosomal System in Parkinson’s Disease: Expanding the Horizon;Journal of Molecular Biology;2023-06
2. Relationship between polymorphism of receptor SCARB2 gene and clinical severity of enterovirus-71 associated hand-foot-mouth disease;Virology Journal;2021-06-30
3. Genetics variants and expression of the SCARB2 gene in the pathogenesis of Parkinson's disease in Russia;Neuroscience Letters;2021-01
4. SCARB2 variants and glucocerebrosidase activity in Parkinson’s disease;npj Parkinson's Disease;2016-03-10
5. No association of FAM47E rs6812193, SCARB2 rs6825004 and STX1B rs4889603 polymorphisms with Parkinson’s disease in a Chinese Han population;Journal of Neural Transmission;2015-07-30
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