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Journal Article
Review
Idiopathic, myoclonic and Dopa-responsive dystonia.
Current Opinion in Neurology 1997 August
The clinical manifestations and the present status of our knowledge of the genetics of the idiopathic, myoclonic and Dopa-responsive dystonias are reviewed. The relevance of recent genetic findings to the classification of the idiopathic dystonias and to the molecular pathogenesis of Dopa-responsive dystonia are emphasized.
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