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Sensorimotor tests unmask a phenotype in the DYT1 knock-in mouse model of dystonia
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We established a behavioural readout for neuronal dysfunction in DYT1 KI mice.

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DYT1 KI mice exhibited sensorimotor deficits in the adhesive removal test.

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Deficits were detected in a complex rotating beam test with changing sensory input.

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Deficits may reflect previously shown cerebellothalamocortical tract alterations.

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