Dysferlin mutations in LGMD2B, Miyoshi myopathy, and atypical dysferlinopathies-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Dysferlin mutations in LGMD2B, Miyoshi myopathy, and atypical dysferlinopathies

Published:2005 Issue:2 Volume:26 Page:165-165
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Nguyen Karine,Bassez Guillaume,Bernard Rafaëlle,Krahn Martin,Labelle Véronique,Figarella-Branger Dominique,Pouget Jean,Hammouda El Hadi,Béroud Christophe,Urtizberea Andoni,Eymard Bruno,Leturcq France,Lévy Nicolas

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Cited by 105 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. Pathophysiological role of connexin and pannexin hemichannels in neuromuscular disorders;The Journal of Physiology;2024-08-22

2. Limb Girdle Muscular Dystrophy Type 2B (LGMD2B): Diagnosis and Therapeutic Possibilities;International Journal of Molecular Sciences;2024-05-21

3. The Dysferlinopathies Conundrum: Clinical Spectra, Disease Mechanism and Genetic Approaches for Treatments;Biomolecules;2024-02-21

4. Dysferlinopathy in Tunisia: clinical spectrum, genetic background and prognostic profile;Neuromuscular Disorders;2023-10

5. Portrait of Dysferlinopathy: Diagnosis and Development of Therapy;Journal of Clinical Medicine;2023-09-16

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