Article
The Q175 mouse model of Huntington's disease shows gene dosage- and age-related decline in circadian rhythms of activity and sleep.
PloS one - 1 Jan 2013
Loh Dawn H, Kudo Takashi, Truong Danny, Wu Yingfei, Colwell Christopher S
Abstract excerpt
Sleep and circadian disruptions are commonly reported by patients with neurodegenerative diseases, suggesting these may be an endophenotype of the disorders. Several mouse models of Huntington's disease (HD) that recapitulate the disease progression and motor dysfunction of HD also exhibit sleep...
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