Genetic defects are common in myopathies with tubular aggregates

Author:

Gang Qiang1234ORCID,Bettencourt Conceição56,Brady Stefen7,Holton Janice L.45,Healy Estelle G.8,McConville John9,Morrison Patrick J.10,Ripolone Michela11,Violano Raffaella11,Sciacco Monica11,Moggio Maurizio11,Mora Marina12,Mantegazza Renato12ORCID,Zanotti Simona12,Wang Zhaoxia12ORCID,Yuan Yun12,Liu Wei‐wei13,Beeson David13,Hanna Michael34,Houlden Henry3414

Affiliation:

1. Department of Neurology Peking University First Hospital 8 Xishiku Street, Xicheng District Beijing 100034 China

2. Beijing Key Laboratory of Neurovascular Disease Discovery Beijing 100034 China

3. Department of Neuromuscular Diseases UCL Queen Square Institute of Neurology Queen Square London UK

4. MRC Centre for Neuromuscular Diseases UCL Queen Square Institute of Neurology Queen Square London UK

5. Queen Square Brain Bank for Neurological Disorders London UK

6. Department of Neurodegenerative Disease UCL Queen Square Institute of Neurology Queen Square London UK

7. Oxford Muscle Service John Radcliffe Hospital Oxford UK

8. Department of Neuropathology Royal Victoria Hospital Belfast Northern Ireland

9. Department of Neurology Belfast City Hospital Belfast BT9 7AB UK

10. Department of Genetic Medicine Belfast City Hospital Belfast BT9 7AB UK

11. Neuromuscular and Rare Diseases Unit Department of Neuroscience IRCCS Foundation Ca’ Granda Ospedale Maggiore Policlinico Dino Ferrari Centre University of Milan Milan Italy

12. Neuromuscular Diseases and Neuroimmunology Unit Fondazione IRCCS Isitituto Neurologico C. Besta Milano Italy

13. Neurosciences Group Nuffield Department of Clinical Neurosciences Weatherall Institute of Molecular Medicine University of Oxford Oxford UK

14. Neurogenetics Laboratory UCL Queen Square Institute of Neurology Queen Square WC1N 3BG London UK

Funder

Medical Research Council

Multiple System Atrophy Trust

National Natural Science Foundation of China

Wellcome

Publisher

Wiley

Subject

Neurology (clinical),General Neuroscience

Cited by 10 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

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