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Genetic mouse models of Huntington’s disease: focus on electrophysiological mechanisms
The discovery of the HD (Huntington’s disease) gene in 1993 led to the creation of genetic mouse models of the disease and opened the doors for mechanistic studies. In particular, the early changes and progression of the disease could be followed and examined systematically. The present review focus...
| Autores principales: | , , , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
American Society for Neurochemistry
2010
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2850512/ https://www.ncbi.nlm.nih.gov/pubmed/20396376 http://dx.doi.org/10.1042/AN20090058 |