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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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| Veröffentlicht in: | Exp Neurol |
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| 1. Verfasser: | |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
2008
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| Schlagworte: | |
| Online Zugang: | 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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