A case of vanishing white matter disease due to the c.260C > T(p.Ala87Val) EIF2B3 mutation

A case of vanishing white matter disease due to the c.260C > T(p.Ala87Val) EIF2B3 mutation / L. Ghezzi, M.T. Bassi, A.M. Pietroboni, G.G. Fumagalli, A. Arighi, M. Rango, M. De Riz, F. Jacini, D. Galimberti, N. Bresolin, E. Scarpini. - In: JOURNAL OF ALZHEIMER'S DISEASE. - ISSN 1387-2877. - 29:suppl.1(2012), pp. 69-69. (Intervento presentato al 7. convegno Congresso Sindem: Italian Association for the study of dementia linked to the Italian neurological society (SIN) tenutosi a Napoli nel 2012) [10.3233/JAD-2012-129000].