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Predominant dystonia with marked cerebellar atrophy: A rare phenotype in familial dystonia
Le Ber, I., Clot, F., Vercueil, L., Camuzat, A., Viemont, M., Benamar, N., De Liege, P., Ouvrard-Hernandez, A. M., Pollak, P., Stevanin, G., Brice, A., Durr, A.Volume:
67
Language:
english
Journal:
Neurology
DOI:
10.1212/01.wnl.0000244484.60489.50
Date:
November, 2006
File:
PDF, 414 KB
english, 2006