Author:
Gasser T.,Wszolek Z. K.,Trofatter J.,Ozelius L.,Uitti R. J.,Lee C. S.,Gusella J.,Pfeiffer R. F.,Calne D. B.,Breakefield X. O.
Subject
Clinical Neurology,Neurology
Reference43 articles.
1. et al.: Hereditary variations in the monoamine oxidase as a risk factor for Parkinson's disease. Mov Disord (in press)
2. Debrisoquine hydroxylase gene polymorphism and susceptibility to Parkinson's disease
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