Decreased number of striatal cholinergic interneurons and motor deficits in dopamine receptor 2-expressing-cell-specific Dyt1 conditional knockout mice

DYT1 early-onset generalized torsion dystonia is a hereditary movement disorder characterized by abnormal postures and repeated movements. It is caused mainly by a heterozygous trinucleotide deletion in DYT1/TOR1A, coding for torsinA. The mutation may lead to a partial loss of torsinA function. Func...

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Publicat a:Neurobiol Dis
Autors principals: Yokoi, Fumiaki, Oleas, Janneth, Xing, Hong, Liu, Yuning, Dexter, Kelly M., Misztal, Carly, Gerard, Melinda, Efimenko, Iakov, Lynch, Patrick, Villanueva, Matthew, Alsina, Raul, Krishnaswamy, Shiv, Vaillancourt, David E., Li, Yuqing
Format: Artigo
Idioma:Inglês
Publicat: 2019
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Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7323754/
https://ncbi.nlm.nih.gov/pubmed/31618684
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nbd.2019.104638
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