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Alterations in striatal synaptic transmission are consistent across genetic mouse models of Huntington's disease
Since the identification of the gene responsible for HD (Huntington's disease), many genetic mouse models have been generated. Each employs a unique approach for delivery of the mutated gene and has a different CAG repeat length and background strain. The resultant diversity in the genetic cont...
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| Auteurs principaux: | , , |
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| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
American Society for Neurochemistry
2010
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2888168/ https://ncbi.nlm.nih.gov/pubmed/20585470 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/AN20100007 |
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