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Earlier onset of motor deficits in mice with double mutations in Dyt1 and Sgce
DYT1 early-onset generalized torsion dystonia is an inherited movement disorder caused by mutations in DYT1 coding for torsinA with ∼30% penetrance. Most of the DYT1 dystonia patients exhibit symptoms during childhood and adolescence. On the other hand, DYT1 mutation carriers without symptoms during...
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| Главные авторы: | , , , , , |
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| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Oxford University Press
2010
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2981491/ https://ncbi.nlm.nih.gov/pubmed/20627944 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/jb/mvq078 |
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