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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...

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Detaylı Bibliyografya
Asıl Yazarlar: Cepeda, Carlos, Cummings, Damian M, André, Véronique M, Holley, Sandra M, Levine, Michael S
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: American Society for Neurochemistry 2010
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2850512/
https://ncbi.nlm.nih.gov/pubmed/20396376
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/AN20090058
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