PLA2G6 mutations cause motor dysfunction phenotypes of young-onset dystonia–parkinsonism type 14 and can be relieved by DHA treatment in animal models-Reference-Cited by-同舟云学术

PLA2G6 mutations cause motor dysfunction phenotypes of young-onset dystonia–parkinsonism type 14 and can be relieved by DHA treatment in animal models

Published:2021-12 Issue: Volume:346 Page:113863
ISSN:0014-4886
Container-title:Experimental Neurology
language:en
Short-container-title:Experimental Neurology

Author:

Yeh Tu-Hsueh,Liu Han-Fang,Chiu Ching-Chi,Cheng Mei-Ling,Huang Guo-Jen,Huang Yin-Cheng,Liu Yu-Chien,Huang Ying-Zu,Lu Chin-Song,Chen Yi-Chieh,Chen Hao-Yuan,Cheng Yi-Chuan

Funder

Chang Gung Memorial Hospital

Chang Gung Medical Foundation

Ministry of Science and Technology, Taiwan

Taipei Medical University

Publisher

Elsevier BV

Subject

Developmental Neuroscience,Neurology

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