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Changes in striatal activity and functional connectivity in a mouse model of Huntington's disease
Hereditary Huntington’s disease (HD) is associated with progressive motor, cognitive and psychiatric symptoms. A primary consequence of the HD mutation is the preferential loss of medium spiny projection cells with relative sparing of local interneurons in the striatum. In addition, among GABAergic...
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| Vydáno v: | PLoS One |
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| Hlavní autoři: | , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Public Library of Science
2017
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5608247/ https://ncbi.nlm.nih.gov/pubmed/28934250 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0184580 |
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