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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:J Neurosci
Autors principals: Sharma, Nutan, Baxter, Mark G., Petravicz, Jeremy, Bragg, D. Cristopher, Schienda, Alonna, Standaert, David G., Breakefield, Xandra O.
Format: Artigo
Idioma:Inglês
Publicat: Society for Neuroscience 2005
Matèries:
Brief Communications
Accés en línia: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
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars