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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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| Publicado no: | J Neurosci |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Society for Neuroscience
2005
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| Assuntos: | |
| Acesso em linha: | 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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