Mutation in ε-Sarcoglycan Induces a Myoclonus-Dystonia Syndrome-Like Movement Disorder in Mice-Reference-Cited by-同舟云学术

Mutation in ε-Sarcoglycan Induces a Myoclonus-Dystonia Syndrome-Like Movement Disorder in Mice

Published:2020-12-23 Issue:3 Volume:37 Page:311-322
ISSN:1673-7067
Container-title:Neuroscience Bulletin
language:en
Short-container-title:Neurosci. Bull.

Author:

Li Jiao,Liu Yiqiong^ORCID,Li Qin,Huang Xiaolin,Zhou Dingxi,Xu Hanjian,Zhao Feng,Mi Xiaoxiao,Wang Ruoxu,Jia Fan,Xu Fuqiang,Yang Jing,Liu Dong,Deng Xuliang,Zhang Yan^ORCID

Publisher

Springer Science and Business Media LLC

Subject

General Medicine,Physiology,General Neuroscience

Link

http://link.springer.com/content/pdf/10.1007/s12264-020-00612-5.pdf

Reference36 articles.

1. Kinugawa K, Vidailhet M, Clot F, Apartis E, Grabli D, Roze E. Myoclonus-dystonia: an update. Mov Disord 2009, 24: 479–489.

2. Phukan J, Albanese A, Gasser T, Warner T. Primary dystonia and dystonia-plus syndromes: clinical characteristics, diagnosis, and pathogenesis. Lancet Neurol 2011, 10: 1074–1085.

3. Popa T, Milani P, Richard A, Hubsch C, Brochard V, Tranchant C et al. The neurophysiological features of myoclonus-dystonia and differentiation from other dystonias. JAMA Neurol 2014, 71: 612–619.

4. Roze E, Apartis E, Clot F, Dorison N, Thobois S, Guyant-Marechal L, et al. Myoclonus-dystonia: clinical and electrophysiologic pattern related to SGCE mutations. Neurology 2008, 70: 1010–1016.

5. Asmus F, Gasser T. Inherited myoclonus-dystonia. Adv Neurol 2004, 94: 113–119.

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