Proline-rich transmembrane protein 2- negative paroxysmal kinesigenic dyskinesia: Clinical and genetic analyses of 163 patients-Reference-Cited by-全球学者库

Proline-rich transmembrane protein 2- negative paroxysmal kinesigenic dyskinesia: Clinical and genetic analyses of 163 patients

Published:2018-01-22 Issue:3 Volume:33 Page:459-467
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Tian Wo-Tu¹,Huang Xiao-Jun¹,Mao Xiao²,Liu Qing³,Liu Xiao-Li¹,Zeng Sheng²,Guo Xia-Nan³,Shen Jun-Yi¹,Xu Yang-Qi¹,Tang Hui-Dong¹,Yin Xiao-Meng²,Zhang Mei⁴,Tang Wei-Guo⁵,Liu Xiao-Rong⁶,Tang Bei-Sha²,Chen Sheng-Di¹,Cao Li¹

Affiliation:

1. Department of Neurology and Institute of Neurology, Rui Jin Hospital & Rui Jin Hospital North; Shanghai Jiao Tong University School of Medicine; Shanghai China

2. Department of Neurology; Xiangya Hospital, Central South University, State Key Laboratory of Medical Genetics; Changsha Hunan Province China

3. Department of Neurology; Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College; Beijing China

4. Department of Neurology; Huainan First People's Hospital affiliated to Bengbu Medical College; Huainan Anhui Province China

5. Department of Neurology; Zhoushan Hospital; Zhoushan Zhejiang Province China

6. Institute of Neuroscience of the Second Affiliated Hospital of Guangzhou Medical University; Guangzhou Guangdong Province China

Funder

National Natural Science Foundation of China

Shanghai Municipal Education Commission-Gaofeng Clinical Medicine

Interdisciplinary Project of Shanghai Jiao Tong University

State Key Program of National Natural Science Foundation of China

Science Research Project of Shanghai Municipal Commission of Health and Family Planning

Guangdong Provincial Department of Education

Guangzhou Science Research Project

Science and Information Technology Bureau of Guangzhou

Technology Research Project in the Public Interest of Zhejiang Province

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mds.27274/fullpdf

Reference39 articles.

1. Clinical evaluation of idiopathic paroxysmal kinesigenic dyskinesia: new diagnostic criteria;Bruno;Neurology,2004

2. Paroxysmal dyskinesias;Bhatia;Mov Disord,2011

3. PRRT2 mutation correlated with phenotype of paroxysmal kinesigenic dyskinesia and drug response;Li;Neurology,2013

4. Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesias;Wang;Brain,2011

5. Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia;Chen;Nat Genet,2011

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