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Cortical and Striatal Circuits in Huntington’s Disease
Huntington’s disease (HD) is a hereditary neurodegenerative disorder that typically manifests in midlife with motor, cognitive, and/or psychiatric symptoms. The disease is caused by a CAG triplet expansion in exon 1 of the huntingtin gene and leads to a severe neurodegeneration in the striatum and c...
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| Publicat a: | Front Neurosci |
|---|---|
| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Frontiers Media S.A.
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7025546/ https://ncbi.nlm.nih.gov/pubmed/32116525 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnins.2020.00082 |
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