Mutation of FA2H underlies a complicated form of hereditary spastic paraplegia (SPG35)-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Mutation of FA2H underlies a complicated form of hereditary spastic paraplegia (SPG35)

Published:2010-01-26 Issue:4 Volume:31 Page:E1251-E1260
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Dick Katherine J.,Eckhardt Matthias,Paisán-Ruiz Coro,Alshehhi Aisha Alkhayat,Proukakis Christos,Sibtain Naomi A.,Maier Helena,Sharifi Reza,Patton Michael A.,Bashir Wafa,Koul Roshan,Raeburn Sandy,Gieselmann Volkmar,Houlden Henry,Crosby Andrew H.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/humu.21205/fullpdf

Cited by 171 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. Medical magnetic resonance imaging publications in Arab countries: A 25-year bibliometric analysis;Heliyon;2024-04

2. A Novel Homozygous Deletion Including Exon 1 of FA2H Gene Causes Spastic Paraplegia-35: Genetic and Lipidomics Analysis of the Patients;Pediatric Neurology;2024-03

3. Hereditary spastic paraplegia type 35 in a Turkish girl with fatty acid hydroxylase-associated neurodegeneration;Journal of Pediatric Endocrinology and Metabolism;2024-02-06

4. Ataxia and spasticity;Neurogenetics for the Practitioner;2024

5. Novel Homozygous FA2H Variant Causing the Full Spectrum of Fatty Acid Hydroxylase-Associated Neurodegeneration (SPG35);Genes;2023-12-20

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