학술논문
A rare truncating mutation in ADH1C (G78stop) shows significant association with Parkinson disease in a large international sample
Document Type
Article
Author
Buervenich, S.; Carmine, A.; Galter, D.; Olson, L.; Anvret, M.; Sydow, O.; McMahon, F.J.; Shahabi, H.N.; Nissbrandt, H.; Johnels, B.; Holmberg, B.; Ahlberg, J.; Eerola, J.; Tienari, P.J.; Hellström, O.; Matsuura, T.; Ashizawa, T.; Wüllner, U.; Klockgether, T.; Zimprich, A.; Gasser, T.; Hanson, M.; Waseem, S.; Singleton, A.
Source
In: Archives of Neurology . (Archives of Neurology, January 2005, 62(1):74-78)
Subject
Language
English
ISSN
00039942