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Reduced Expression of Foxp1 as a Contributing Factor in Huntington's Disease
Huntington's disease (HD) is an inherited neurodegenerative disease caused by a polyglutamine expansion in the huntington protein (htt). The neuropathological hallmark of HD is the loss of neurons in the striatum and, to a lesser extent, in the cortex. Foxp1 is a member of the Forkhead family o...
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| Publicado en: | J Neurosci |
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| Autores principales: | , , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Society for Neuroscience
2017
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5511885/ https://ncbi.nlm.nih.gov/pubmed/28550168 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.3612-16.2017 |
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