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TorsinA hypofunction causes abnormal twisting movements and sensorimotor circuit neurodegeneration
Lack of a preclinical model of primary dystonia that exhibits dystonic-like twisting movements has stymied identification of the cellular and molecular underpinnings of the disease. The classical familial form of primary dystonia is caused by the DYT1 (ΔE) mutation in TOR1A, which encodes torsinA, A...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
American Society for Clinical Investigation
2014
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4071385/ https://ncbi.nlm.nih.gov/pubmed/24937429 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI72830 |
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