Novel insights into the pathogenesis of DYT1 dystonia from induced patient-derived neurons  

作　　者：Baojin Ding 

机构地区：[1]Department of Biology,University of Louisiana at Lafayette,Lafayette,LA,USA

出　　处：《Neural Regeneration Research》2022年第3期561-562,共2页中国神经再生研究（英文版）

基　　金：supported by National Institute of Neurological Diseases and Stroke,No.NIH/NINDS NS112910 (to BD);Department of Defense (DoD) Peer Reviewed Medical Research Program (PRMRP) Discovery Award,No.W81XWH2010186 (to BD)。

摘　　要：Dystonia is a common movement disorder characterized by sustained or intermittent muscle contractions causing abnormal movements and/or postures(Keller Sarmiento and Mencacci,2021).The dystonic syndromes are classified as primary dystonia(dystonia is the only motor feature without tremor) and the secondary dystonia(dystonia is combined with other movement disorders,such as Parkinsonism).

关 键 词：SUSTAINED Keller DYT1 

分 类 号：R746[医药卫生—神经病学与精神病学]