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The abnormal firing of Purkinje cells in the knockin mouse model of DYT1 dystonia

DYT1 dystonia is an inherited movement disorder caused by a heterozygous trinucleotide (GAG) deletion in DYT1/TOR1A, coding for torsinA. Growing evidence suggests that the cerebellum plays a role in the pathogenesis of dystonia. Brain imaging of both DYT1 dystonia patients and animal models show abn...

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Detalhes bibliográficos
Publicado no:Brain Res Bull
Main Authors: Liu, Yuning, Xing, Hong, Wilkes, Bradley J., Yokoi, Fumiaki, Chen, Huanxin, Vaillancourt, David E., Li, Yuqing
Formato: Artigo
Idioma:Inglês
Publicado em: 2020
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7674218/
https://ncbi.nlm.nih.gov/pubmed/32976982
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.brainresbull.2020.09.011
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