Lack of association between TOR1A and THAP1 mutations and sporadic adult-onset primary focal dystonia in a Chinese population-Reference-Cited by-同舟云学术

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Lack of association between TOR1A and THAP1 mutations and sporadic adult-onset primary focal dystonia in a Chinese population

Published:2016-03 Issue: Volume:142 Page:26-30
ISSN:0303-8467
Container-title:Clinical Neurology and Neurosurgery
language:en
Short-container-title:Clinical Neurology and Neurosurgery

Author:

Wang Lei,Duan Chenchi,Gao Yuan,Xu Wei,Ding Jianqing,Liu Victoria T.,Wu Yiwen

Funder

National Natural Science Foundation of China

Innovation Program of Shanghai Municipal Education Commission

Med-X Project of Shanghai Jiaotong University

Science and Technology Commission of Shanghai Municipality

Publisher

Elsevier BV

Subject

Clinical Neurology,General Medicine,Surgery

Reference24 articles.

1. Classification of movement disorders;Fahn;Mov. Disord.,2011

2. Classification of dystonia;Fahn;Adv. Neurol.,1998

3. The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein;Ozelius;Nat. Genet.,1997

4. The role of DYT1 in primary torsion dystonia in Europe;Valente;Brain,1998

5. DYT1 mutation in Japanese patients with primary torsion dystonia;Matsumoto;NeuroReport,2001

Cited by 2 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. Risk Factor Genes in Patients with Dystonia: A Comprehensive Review;TREMOR OTHER HYPERK;2019

2. The Role of TOR1A Polymorphisms in Dystonia: A Systematic Review and Meta-Analysis;PLOS ONE;2017-01-12

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