Refinement of the SPG9 locus on chromosome 10q23.3-24.2 and exclusion of candidate genes-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Refinement of the SPG9 locus on chromosome 10q23.3-24.2 and exclusion of candidate genes

Published:2008-05 Issue:5 Volume:15 Page:520-524
ISSN:1351-5101
Container-title:European Journal of Neurology
language:en
Short-container-title:Eur J Neurol

Author:

Panza E.,Pippucci T.,Cusano R.,Lo Nigro C.,Pradella L.,Contardi S.,Rouleau G. A.,Stevanin G.,Ravazzolo R.,Liguori R.,Montagna P.,Romeo G.,Seri M.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1468-1331.2008.02117.x/fullpdf

Reference18 articles.

1. Pure hereditary spastic paraplegia.

2. Science in motion: common molecular pathological themes emerge in the hereditary spastic paraplegias

3. Hereditary Spastic Paraplegias

4. New locus for hereditary spastic paraplegia maps to chromosome 1p31.1-1p21.1

Cited by 7 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. Hereditary spastic paraplegia: Genetic heterogeneity and common pathways;Experimental Neurology;2022-11

2. Novel Type of Complicated Autosomal Dominant Hereditary Spastic Paraplegia Associated with Congenital Distal Arthrogryposis Type I;Brain Sciences;2018-07-19

3. Hereditary Spastic Paraplegia;Neurodegeneration;2017-02-18

4. The Genetics of GER and GERD;Esophageal and Gastric Disorders in Infancy and Childhood;2017

5. ALDH18A1gene mutations cause dominant spastic paraplegia SPG9: loss of function effect and plausibility of a dominant negative mechanism;Brain;2015-08-21

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