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Distinct histological alterations of cortical interneuron types in mouse models of Huntington’s disease
Huntington’s disease (HD) is a debilitating hereditary motor disorder caused by an expansion of the CAG triplet repeat in the Huntingtin gene. HD causes neurodegeneration particularly in the basal ganglia and neocortex. In the cortex, glutamatergic pyramidal neurons are known to be severely affected...
Autores principales: | Voelkl, Kerstin, Schulz-Trieglaff, Elena Katharina, Klein, Rüdiger, Dudanova, Irina |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9549412/ https://www.ncbi.nlm.nih.gov/pubmed/36225731 http://dx.doi.org/10.3389/fnins.2022.1022251 |
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