GRN Asp22fs mutation is associated with highly variable age at onset, clinical phenotype and brain atrophy

GRN Asp22fs mutation is associated with highly variable age at onset, clinical phenotype and brain atrophy / A. Pietroboni, G. Fumagalli, L. Ghezzi, C. Fenoglio, F. Cortini, M. Serpente, C. Cantoni, E. Rotondo, P. Corti, N. Bresolin, D. Galimberti, E. Scarpini. - In: NEUROLOGICAL SCIENCES. - ISSN 1590-1874. - (2010). ((Intervento presentato al convegno XLI Congress of the Italian Neurological Society.