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U-Fiber Leukoencephalopathy Due to a Novel Mutation in the TACO1 Gene.
Sferruzza, Giacomo; Del Bondio, Andrea; Citterio, Andrea; Vezzulli, Paolo; Guerrieri, Simone; Radaelli, Marta; Martinelli Boneschi, Filippo; Filippi, Massimo; Maltecca, Francesca; Bassi, Maria Teresa; Scarlato, Marina.
Afiliación
  • Sferruzza G; Department of Neurology (G.S., S.G., M.F., M.S.), and Mitochondrial Dysfunctions in Neurodegeneration Unit (A.D.B., F.M.), Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan; Laboratory of Molecular Biology (A.C., M.T.B.), Scientific Institute IRCCS E. Medea, Bosisio Parini, Le
  • Del Bondio A; Department of Neurology (G.S., S.G., M.F., M.S.), and Mitochondrial Dysfunctions in Neurodegeneration Unit (A.D.B., F.M.), Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan; Laboratory of Molecular Biology (A.C., M.T.B.), Scientific Institute IRCCS E. Medea, Bosisio Parini, Le
  • Citterio A; Department of Neurology (G.S., S.G., M.F., M.S.), and Mitochondrial Dysfunctions in Neurodegeneration Unit (A.D.B., F.M.), Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan; Laboratory of Molecular Biology (A.C., M.T.B.), Scientific Institute IRCCS E. Medea, Bosisio Parini, Le
  • Vezzulli P; Department of Neurology (G.S., S.G., M.F., M.S.), and Mitochondrial Dysfunctions in Neurodegeneration Unit (A.D.B., F.M.), Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan; Laboratory of Molecular Biology (A.C., M.T.B.), Scientific Institute IRCCS E. Medea, Bosisio Parini, Le
  • Guerrieri S; Department of Neurology (G.S., S.G., M.F., M.S.), and Mitochondrial Dysfunctions in Neurodegeneration Unit (A.D.B., F.M.), Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan; Laboratory of Molecular Biology (A.C., M.T.B.), Scientific Institute IRCCS E. Medea, Bosisio Parini, Le
  • Radaelli M; Department of Neurology (G.S., S.G., M.F., M.S.), and Mitochondrial Dysfunctions in Neurodegeneration Unit (A.D.B., F.M.), Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan; Laboratory of Molecular Biology (A.C., M.T.B.), Scientific Institute IRCCS E. Medea, Bosisio Parini, Le
  • Martinelli Boneschi F; Department of Neurology (G.S., S.G., M.F., M.S.), and Mitochondrial Dysfunctions in Neurodegeneration Unit (A.D.B., F.M.), Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan; Laboratory of Molecular Biology (A.C., M.T.B.), Scientific Institute IRCCS E. Medea, Bosisio Parini, Le
  • Filippi M; Department of Neurology (G.S., S.G., M.F., M.S.), and Mitochondrial Dysfunctions in Neurodegeneration Unit (A.D.B., F.M.), Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan; Laboratory of Molecular Biology (A.C., M.T.B.), Scientific Institute IRCCS E. Medea, Bosisio Parini, Le
  • Maltecca F; Department of Neurology (G.S., S.G., M.F., M.S.), and Mitochondrial Dysfunctions in Neurodegeneration Unit (A.D.B., F.M.), Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan; Laboratory of Molecular Biology (A.C., M.T.B.), Scientific Institute IRCCS E. Medea, Bosisio Parini, Le
  • Bassi MT; Department of Neurology (G.S., S.G., M.F., M.S.), and Mitochondrial Dysfunctions in Neurodegeneration Unit (A.D.B., F.M.), Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan; Laboratory of Molecular Biology (A.C., M.T.B.), Scientific Institute IRCCS E. Medea, Bosisio Parini, Le
  • Scarlato M; Department of Neurology (G.S., S.G., M.F., M.S.), and Mitochondrial Dysfunctions in Neurodegeneration Unit (A.D.B., F.M.), Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan; Laboratory of Molecular Biology (A.C., M.T.B.), Scientific Institute IRCCS E. Medea, Bosisio Parini, Le
Neurol Genet ; 7(2): e573, 2021 Apr.
Article en En | MEDLINE | ID: mdl-33709035

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Neurol Genet Año: 2021 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Neurol Genet Año: 2021 Tipo del documento: Article