Impaired Motor Learning in Mice Expressing TorsinA with the DYT1 Dystonia Mutation

Primary early-onset generalized dystonia is an autosomal dominant disorder caused by a deletion (ΔGAG) in the DYT1 gene encoding torsinA. The gene defect has incomplete penetrance, with ∼30% of carriers developing clinically evident dystonia. We describe lines of transgenic mice that express either...

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Detaylı Bibliyografya
Yayımlandı:J Neurosci
Asıl Yazarlar: Sharma, Nutan, Baxter, Mark G., Petravicz, Jeremy, Bragg, D. Cristopher, Schienda, Alonna, Standaert, David G., Breakefield, Xandra O.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Society for Neuroscience 2005
Konular:
Brief Communications
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6725000/
https://ncbi.nlm.nih.gov/pubmed/15930383
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.0855-05.2005
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