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Idiopathic, myoclonic and Dopa-responsive dystonia
1Department of Neurology, Klinikum Grosshadern, Ludwig-Maximilians-Universität, München, Germany.
Current Opinion in Neurology
|August 1, 1997
Abstract:
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.