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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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Détails bibliographiques
Auteurs principaux: Cummings, Damian M, Cepeda, Carlos, Levine, Michael S
Format: Artigo
Langue:Inglês
Publié: American Society for Neurochemistry 2010
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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