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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Detalles Bibliográficos
Autores principales: Cummings, Damian M, Cepeda, Carlos, Levine, Michael S
Formato: Texto
Lenguaje:English
Publicado: American Society for Neurochemistry 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2888168/
https://www.ncbi.nlm.nih.gov/pubmed/20585470
http://dx.doi.org/10.1042/AN20100007

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2888168/
https://www.ncbi.nlm.nih.gov/pubmed/20585470
http://dx.doi.org/10.1042/AN20100007

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