Clinical feature and DYT1 mutation screening in primary dystonia patients from South-West China

Author:

Zhang S.-S.,Fang D.-F.,Hu X.-H.,Burgunder J.-M.,Chen X.-P.,Zhang Y.-W.,Shang H.-F.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference44 articles.

Cited by 21 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. Investigating DYT1 in a Taiwanese dystonia cohort;Journal of the Formosan Medical Association;2022-01

2. Complex Medical Diagnoses With an Underlying Dental Etiology;Advances in Medical Technologies and Clinical Practice;2020

3. Quality of life in idiopathic dystonia: a systematic review;Journal of Neurology;2018-11-20

4. Non-motor disorders in patients with muscular dystonia;Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova;2018

5. Association analysis of four candidate genetic variants with sporadic amyotrophic lateral sclerosis in a Chinese population;Neurological Sciences;2014-02-04

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