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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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| Publicado no: | Exp Neurol |
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| Autor principal: | |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2008
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| Assuntos: | |
| Acesso em linha: | 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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