A rare truncating mutation in ADH1C (G78Stop) shows significant association with Parkinson disease in a large international sample.

Silvia Buervenich,Andrea Carmine,D. Galter,H. N. Shahabi,B. Johnels,B. Holmberg,Jarl Ahlberg,H. Nissbrandt,J. Eerola,O. Hellström,P. Tienari,T. Matsuura,T. Ashizawa,U. Wüllner,T. Klockgether,A. Zimprich,T. Gasser,M. Hanson,Shamaila Waseem,A. Singleton,F. McMahon,M. Anvret,O. Sydow,L. Olson

Published 2005 in Archives of Neurology

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