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Corticobasal syndrome and primary progressive aphasia as manifestations of LRRK2 gene mutations
Chen-Plotkin, A. S., Yuan, W., Anderson, C., Wood, E. M., Hurtig, H. I., Clark, C. M., Miller, B. L., Lee, V. M.-Y., Trojanowski, J. Q., Grossman, M., Deerlin, V. M. V.Volume:
70
Langue:
english
Journal:
Neurology
DOI:
10.1212/01.wnl.0000280574.17166.26
Date:
February, 2008
Fichier:
PDF, 513 KB
english, 2008