APRRT2variant in a Chinese family with paroxysmal kinesigenic dyskinesia and benign familial infantile seizures results in loss of interaction withSTX1B-Reference-Cited by-同舟云学术

APRRT2variant in a Chinese family with paroxysmal kinesigenic dyskinesia and benign familial infantile seizures results in loss of interaction withSTX1B

Published:2018-07-15 Issue:8 Volume:59 Page:1621-1630
ISSN:0013-9580
Container-title:Epilepsia
language:en
Short-container-title:Epilepsia

Author:

Ma Hongying¹,Feng Shenglei¹,Deng Xuejun²,Wang Li¹,Zeng Sheng³,Wang Cheng¹,Ma Xixiang¹,Sun Hao¹,Chen Rui¹,Du Shiyue¹,Mao Jinglin¹,Zhang Xianwei⁴,Ma Cong¹,Jiang Hong³,Zhang Luoying¹,Tang Beisha³,Liu Jing Yu¹

Affiliation:

1. Key Laboratory of Molecular Biophysics of the Ministry of Education; Center for Human Genome Research; College of Life Science and Technology; Huazhong University of Science and Technology; Wuhan China

2. Department of Neurology; Union Hospital of Huazhong University of Science and Technology; Wuhan China

3. Department of Neurology, Xiangya Hospital; Key Laboratory of Hunan Province in Neurodegenerative Disorders; Central South University; Changsha China

4. Department of Anesthesiology; Tongji Hospital of Huazhong University of Science and Technology; Wuhan China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/epi.14511/fullpdf

Reference37 articles.

1. PRRT2 mutations in paroxysmal dyskinesia patients with variant inheritance and phenotypes;Liu;Genes Brain Behav,2013

2. Paroxysmal dyskinesias;Bhatia;Mov Disord,2011