Differential loss of thalamostriatal and corticostriatal input to striatal projection neuron types prior to overt motor symptoms in the Q140 knock-in mouse model of Huntington's disease.

Front Syst Neurosci · 2014 · PMC4197654 · PMID 25360089

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highly significantno p-value reported

The correlations for progression segment length and stops were highly significant.

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showed a trendno p-value reported

Though they showed a trend toward decline in abundance at 12 months in Q140 mice, the results were variable due to the scarcity of axodendritic corticostriatal terminals in mice.

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