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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發表在:J Neurosci
Main Authors: Sharma, Nutan, Baxter, Mark G., Petravicz, Jeremy, Bragg, D. Cristopher, Schienda, Alonna, Standaert, David G., Breakefield, Xandra O.
格式: Artigo
語言:Inglês
出版: Society for Neuroscience 2005
主題:
Brief Communications
在線閱讀: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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