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Characterization of Atp1a3 mutant mice as a model of rapid-onset dystonia with parkinsonism
Rapid-onset dystonia with parkinsonism (RDP) or DYT12 dystonia is a rare form of primary, generalized dystonia. Patients do not present with any symptoms until triggered by a physiological stressor. Within days, patients will show both dystonia and Parkinson’s disease. Missense mutations resulting i...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2981691/ https://ncbi.nlm.nih.gov/pubmed/20850480 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bbr.2010.09.009 |
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