Intrafamilial variable presentation of CMT2, spastic paraparesis and cognitive impairment caused by a novel autosomal dominant MFN2 mutation

Intrafamilial variable presentation of CMT2, spastic paraparesis and cognitive impairment caused by a novel autosomal dominant MFN2 mutation / S. Ghezzi, R. Del Bo, S. Bonato, G. Airoldi, M.G. D’Angelo, A.C. Turioni, M.T. Bassi, N. Bresolin, G.P. Comi. ((Intervento presentato al convegno 59° Annual Meeting of American Academy of Neurology tenutosi a null nel null.