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In general, dystonias that were formerly classified as primary dystonias, including genetic and focal/segmental idiopathic dystonias, are more amenable to treatment [ The genetic dystonias have been thoroughly reviewed due to their prevalence and the relative ease with which diseases with mendelian inheritance can be interrogated in the genomics era, both through clinical research and with model organisms [ To understand how dystonia network dysfunction manifests, first we will evaluate the acquired dystonias in comparison to network function in idiopathic dystonias

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