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CORTICOBASAL SYNDROME AND PRIMARY PROGRESSIVE APHASIA AS MANIFESTATIONS OF LRRK2 GENE MUTATIONS
Ross, O. A., Toft, M., Haugarvoll, K., Chen-Plotkin, A., Yuan, W., Anderson, C., Wood, E. M., Hurtig, H.I., Clark, C., Miller, B.L., Lee, V.M.-Y., Trojanowski, J.Q., Grossman, M., Van Deerlin, V.M.Volume:
71
Langue:
english
Journal:
Neurology
DOI:
10.1212/01.wnl.0000320511.30222.dd
Date:
July, 2008
Fichier:
PDF, 144 KB
english, 2008