PRRT2 deficiency induces paroxysmal kinesigenic dyskinesia by regulating synaptic transmission in cerebellum-Reference-Cited by-同舟云学术

PRRT2 deficiency induces paroxysmal kinesigenic dyskinesia by regulating synaptic transmission in cerebellum

Published:2017-10-20 Issue:1 Volume:28 Page:90-110
ISSN:1001-0602
Container-title:Cell Research
language:en
Short-container-title:Cell Res

Author:

Tan Guo-He,Liu Yuan-Yuan,Wang Lu,Li Kui,Zhang Ze-Qiang,Li Hong-Fu,Yang Zhong-Fei,Li Yang,Li Dan,Wu Ming-Yue,Yu Chun-Lei,Long Juan-Juan,Chen Ren-Chao,Li Li-Xi,Yin Lu-Ping,Liu Ji-Wei,Cheng Xue-Wen,Shen Qi,Shu You-Sheng,Sakimura Kenji,Liao Lu-Jian,Wu Zhi-Ying,Xiong Zhi-Qi

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Molecular Biology

Link

http://www.nature.com/articles/cr2017128.pdf

Reference55 articles.

1. Bhatia KP . Paroxysmal dyskinesias. Mov Disord 2011; 26:1157–1165.

2. Ebrahimi-Fakhari D, Saffari A, Westenberger A, Klein C . The evolving spectrum of PRRT2-associated paroxysmal diseases. Brain 2015; 138:3476–3495

3. Chen WJ, Lin Y, Xiong ZQ, et al. Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia. Nat Genet 2011; 43:1252–1255.

4. Meneret A, Gaudebout C, Riant F, et al. PRRT2 mutations and paroxysmal disorders. Eur J Neurol 2013; 20:872–878.

5. Schubert J, Paravidino R, Becker F, et al. PRRT2 mutations are the major cause of benign familial infantile seizures. Hum Mutat 2012; 33:1439–1443.

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