Genotype–phenotype correlation in inherited brain myelination defects due to proteolipid protein gene mutations-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Genotype–phenotype correlation in inherited brain myelination defects due to proteolipid protein gene mutations

Published:2000-10-31 Issue:11 Volume:8 Page:837-845
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Cailloux Fabrice, ,Gauthier-Barichard Fernande,Mimault Corinne,Isabelle Valerie,Courtois Virginie,Giraud Geneviève,Dastugue Bernard,Boespflug-Tanguy Odile

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/5200537.pdf

Cited by 172 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. Terra incognita of glial cell dynamics in the etiology of leukodystrophies: Broadening disease and therapeutic perspectives;Life Sciences;2024-10

2. Unlocking the potential of circulating small extracellular vesicles in neurodegenerative disease through targeted biomarkers and advancements in biosensing;Exploration of BioMat-X;2024-04-24

3. An Open-Label Administration of Bioavailable-Form Curcumin in Patients With Pelizaeus-Merzbacher Disease;Pediatric Neurology;2024-02

4. Molecular Pathogenic Mechanisms of Hypomyelinating Leukodystrophies (HLDs);Neurology International;2023-09-11

5. Optical genome mapping in an atypical Pelizaeus-Merzbacher prenatal challenge;Frontiers in Genetics;2023-07-25

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