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Commentary: Dopaminergic dysfunction in DYT1 dystonia

A three-base-pair deletion in the torsinA gene leads to generalized torsion dystonia (DYT1) in humans, an often devastating movement disorder in which voluntary movements are disrupted by sustained muscle spasms and abnormal limb posturing. In a recent issue of Experimental Neurology, Zhao et al. (2...

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Detalles Bibliográficos
Publicado en:Exp Neurol
Autor Principal: Wichmann, Thomas
Formato: Artigo
Idioma:Inglês
Publicado: 2008
Assuntos:
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC4305330/
https://ncbi.nlm.nih.gov/pubmed/18513716
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.expneurol.2008.04.020
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