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Mutated mitofusin 2 presents with intrafamilial variability and brain mitochondrial dysfunction.
Del Bo, R; Moggio, M; Rango, M; Bonato, S; D'Angelo, M G; Ghezzi, S; Airoldi, G; Bassi, M T; Guglieri, M; Napoli, L; Lamperti, C; Corti, S; Federico, A; Bresolin, N; Comi, G P.
Affiliation
  • Del Bo R; Dino Ferrari Centre, Department of Neurological Sciences, University of Milan, IRCCS Foundation Ospedale Maggiore Policlinico Mangiagalli and Regina Elena, Milan, Italy.
Neurology ; 71(24): 1959-66, 2008 Dec 09.
Article in En | MEDLINE | ID: mdl-18946002
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Brain Diseases, Metabolic / Charcot-Marie-Tooth Disease / Cognition Disorders / Mitochondrial Diseases / Mitochondrial Proteins / Membrane Proteins Type of study: Prognostic_studies Limits: Adult / Child / Humans / Male Language: En Journal: Neurology Year: 2008 Document type: Article
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Brain Diseases, Metabolic / Charcot-Marie-Tooth Disease / Cognition Disorders / Mitochondrial Diseases / Mitochondrial Proteins / Membrane Proteins Type of study: Prognostic_studies Limits: Adult / Child / Humans / Male Language: En Journal: Neurology Year: 2008 Document type: Article