Features Differ Between Paroxysmal Kinesigenic Dyskinesia Patients with <scp> <i>PRRT2</i> </scp> and <scp> <i>TMEM151A</i> </scp> Variants-Reference-Cited by-同舟云学术

Features Differ Between Paroxysmal Kinesigenic Dyskinesia Patients with PRRT2 and TMEM151A Variants

Published:2022-01-27 Issue:3 Volume:37 Page:608-613
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Movement Disorders

Author:

Chen Yu‐Lan¹,Chen Dian‐Fu¹,Li Hong‐Fu¹,Wu Zhi‐Ying¹^ORCID

Affiliation:

1. Department of Neurology and Research Center of Neurology in Second Affiliated Hospital and Key Laboratory of Medical Neurobiology of Zhejiang Province Zhejiang University School of Medicine Hangzhou China

Funder

National Natural Science Foundation of China

Zhejiang University

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mds.28939

Reference21 articles.

1. Paroxysmal kinesigenic choreoathetosis: An entity within the paroxysmal choreoathetosis syndrome. Description of 10 cases, including 1 autopsied

2. Clinical evaluation of idiopathic paroxysmal kinesigenic dyskinesia

3. Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia

4. Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesias

5. PRRT2 mutations: A major cause of paroxysmal kinesigenic dyskinesia in the European population

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