APA

Ghezzi L., Scarpini E., Rango M., Arighi A., Bassi M. T., Tenderini E., De Riz M., Jacini F., Fumagalli G. G., Pietroboni A. M., Galimberti D. & Bresolin N. (20130116). A 66-year-old patient with vanishing white matter disease due to the p.Ala87Val EIF2B3 mutation. : Neurology.

Chicago

Ghezzi Laura, Scarpini Elio, Rango Mario, Arighi Andrea, Bassi Maria Teresa, Tenderini Erika, De Riz Milena, Jacini Francesca, Fumagalli Giorgio G, Pietroboni Anna M, Galimberti Daniela and Bresolin Nereo. 20130116. A 66-year-old patient with vanishing white matter disease due to the p.Ala87Val EIF2B3 mutation. : Neurology.

Harvard

Ghezzi L., Scarpini E., Rango M., Arighi A., Bassi M. T., Tenderini E., De Riz M., Jacini F., Fumagalli G. G., Pietroboni A. M., Galimberti D. and Bresolin N. (20130116). A 66-year-old patient with vanishing white matter disease due to the p.Ala87Val EIF2B3 mutation. : Neurology.

MLA

Ghezzi Laura, Scarpini Elio, Rango Mario, Arighi Andrea, Bassi Maria Teresa, Tenderini Erika, De Riz Milena, Jacini Francesca, Fumagalli Giorgio G, Pietroboni Anna M, Galimberti Daniela and Bresolin Nereo. A 66-year-old patient with vanishing white matter disease due to the p.Ala87Val EIF2B3 mutation. : Neurology. 20130116.