Gap junction protein beta 1 (GJB1 ) mutations and central nervous system symptoms in X-linked Charcot-Marie-Tooth disease-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Gap junction protein beta 1 (GJB1 ) mutations and central nervous system symptoms in X-linked Charcot-Marie-Tooth disease

Published:2003-01 Issue:1 Volume:107 Page:31-37
ISSN:0001-6314
Container-title:Acta Neurologica Scandinavica
language:en
Short-container-title:

Author:

Takashima H.,Nakagawa M.,Umehara F.,Hirata K.,Suehara M.,Mayumi H.,Yoshishige K.,Matsuyama W.,Saito M.,Jonosono M.,Arimura K.,Osame M.

Publisher

Wiley

Subject

Neurology (clinical),Neurology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1600-0404.2003.01317.x/fullpdf

Reference38 articles.

1. Genetic and clinical aspects of Charcot-Marie-Tooth disease;Skre;Clin Genet,1974

2. The Charcot-Marie-Tooth syndrome: clinical aspects from a population study in South Wales, UK;MacMillan;Clin Genet,1994

3. Population frequencies of inherited neuromuscular disease-a world survey;Emery;Neuromuscul Disord,1991

4. Charcot-Marie-Tooth neuropathy: from clinical description to molecular genetics;Ionasescu;Muscle Nerve,1995

5. Connexin mutations in X-linked Charcot-Marie-Tooth disease;Bergoffen;Science,1993

Cited by 37 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 and extensive leukoencephalopathy: a case report of a unique phenotype associated with a GJB1/Cx32 p.Pro174Ser variant;BMC Neurology;2024-09-04

2. Genetic research of inherited peripheral neuropathies;Neurology and Clinical Neuroscience;2023-08-06

3. Knock-in mouse models for CMTX1 show a loss of function phenotype in the peripheral nervous system;Experimental Neurology;2023-02

4. New evidence for secondary axonal degeneration in demyelinating neuropathies;Neuroscience Letters;2021-01

5. New novel mutations in Brazilian families with X‐linked Charcot‐Marie‐Tooth disease;Journal of the Peripheral Nervous System;2019-06

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