No abstract is available for this paper.
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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- Publication year
2005
- Venue
Archives of Neurology
- Publication date
Unknown publication date
- Fields of study
Biology, Medicine
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Semantic Scholar, PubMed
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