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Cortical circuit alterations precede motor impairments in Huntington’s disease mice
Huntington’s disease (HD) is a devastating hereditary movement disorder, characterized by degeneration of neurons in the striatum and cortex. Studies in human patients and mouse HD models suggest that disturbances of neuronal function in the neocortex play an important role in disease onset and prog...
Autores principales: | Burgold, Johanna, Schulz-Trieglaff, Elena Katharina, Voelkl, Kerstin, Gutiérrez-Ángel, Sara, Bader, Jakob Maximilian, Hosp, Fabian, Mann, Matthias, Arzberger, Thomas, Klein, Rüdiger, Liebscher, Sabine, Dudanova, Irina |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6488584/ https://www.ncbi.nlm.nih.gov/pubmed/31036840 http://dx.doi.org/10.1038/s41598-019-43024-w |
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