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Disrupted striatal neuron inputs and outputs in Huntington's disease
Huntington's disease (HD) is a hereditary progressive neurodegenerative disorder caused by a CAG repeat expansion in the gene coding for the protein huntingtin, resulting in a pathogenic expansion of the polyglutamine tract in the N‐terminus of this protein. The HD pathology resulting from the...
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| Publicado no: | CNS Neurosci Ther |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5875736/ https://ncbi.nlm.nih.gov/pubmed/29582587 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/cns.12844 |
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