Genetic Background Modulates the Phenotype of a Mouse Model of DYT1 Dystonia

Genetic modifiers of neurological disease

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Early Changes in Cerebellar Physiology Accompany Motor Dysfunction in the Polyglutamine Disease Spinocerebellar Ataxia Type 3

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Cerebellothalamocortical pathway abnormalities in torsinA DYT1 knock-in mice

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Hereditary dystonia as a neurodevelopmental circuit disorder: Evidence from neuroimaging

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A molecular mechanism underlying the neural-specific defect in torsinA mutant mice

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Impairment of bidirectional synaptic plasticity in the striatum of a mouse model of DYT1 dystonia: role of endogenous acetylcholine

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Printor, a Novel TorsinA-interacting Protein Implicated in Dystonia Pathogenesis

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Cerebellothalamocortical Connectivity Regulates Penetrance in Dystonia

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Primary dystonia: molecules and mechanisms

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