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Electromyographic evidence in support of a knock-in mouse model of DYT1 dystonia
BACKGROUND: DYT1 dystonia is an autosomal dominant movement disorder characterized by abnormal, often repetitive, movements, and postures. Its hallmark feature is sustained or intermittent contractions of muscles involving co-contractions of antagonist muscle pairs. The symptoms are relieved with th...
Enregistré dans:
| Publié dans: | Mov Disord |
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| Auteurs principaux: | , , , , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
2016
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5115930/ https://ncbi.nlm.nih.gov/pubmed/27241685 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mds.26677 |
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