TMEM151A as an alternative to PRRT2 in paroxysmal kinesigenic dyskinesia: About three new cases
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Geriatrics and Gerontology,Neurology
Reference6 articles.
1. Paroxysmal movement disorders: recent advances and proposal of a classification system;Zhang;Park. Relat. Disord.,2019
2. TMEM151A variants cause paroxysmal kinesigenic dyskinesia;Li;Cell Discov.,2021
3. TMEM151A variants cause paroxysmal kinesigenic dyskinesia: a large-sample study;Tian;Mov. Disord.,2022
4. PRRT2 mutations: a major cause of paroxysmal kinesigenic dyskinesia in the European population;Méneret;Neurology,2012
5. Features differ between paroxysmal kinesigenic dyskinesia patients with PRRT2 and TMEM151A variants;Chen;Mov. Disord.,2022
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. Paroxysmal Kinesigenic Dyskinesia: Genetics and Pathophysiological Mechanisms;Neuroscience Bulletin;2023-12-13
2. TMEM151A variants associated with paroxysmal kinesigenic dyskinesia;Human Genetics;2023-03-01
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