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Giant axonal neuropathy: a multicenter retrospective study with genotypic spectrum expansion.
Echaniz-Laguna, Andoni; Cuisset, Jean-Marie; Guyant-Marechal, Lucie; Aubourg, Patrick; Kremer, Laurent; Baaloul, Naziha; Verloes, Alain; Beladgham, Kouider; Perrot, Jimmy; Francou, Bruno; Latour, Philippe.
Afiliación
  • Echaniz-Laguna A; Neurology Department, APHP, CHU de Bicêtre, 78 rue du Général Leclerc, 94276, Le Kremlin-Bicêtre Cedex, France. Andoni.echaniz-laguna@aphp.fr.
  • Cuisset JM; French National Reference Center for Rare Neuropathies (NNERF), 94276, Le Kremlin-Bicêtre, France. Andoni.echaniz-laguna@aphp.fr.
  • Guyant-Marechal L; INSERM U1195 Paris-Sud University, 94276, Le Kremlin-Bicêtre, France. Andoni.echaniz-laguna@aphp.fr.
  • Aubourg P; Pediatrics Department, CHU de Lille, Lille, France.
  • Kremer L; Genetics Department, CHU de Rouen, Rouen, France.
  • Baaloul N; Department of Pediatric Neurology, APHP, Bicêtre University Hospital, Le Kremlin-Bicêtre, France.
  • Verloes A; Paris-Sud University, Inserm U 1169, Le Kremlin-Bicêtre, France.
  • Beladgham K; Department of Neurology, Hôpitaux Universitaires, 67098, Strasbourg, France.
  • Perrot J; INSERM U1119, FMTS, UDS, Strasbourg, France.
  • Francou B; , Constantine, Algeria.
  • Latour P; Genetics Department, APHP, Robert Debré Hospital, Paris, France.
Neurogenetics ; 21(1): 29-37, 2020 01.
Article en En | MEDLINE | ID: mdl-31655922
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Proteínas del Citoesqueleto / Neuropatía Axonal Gigante / Mutación Tipo de estudio: Observational_studies / Prognostic_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Neurogenetics Asunto de la revista: GENETICA / NEUROLOGIA Año: 2020 Tipo del documento: Article País de afiliación: Francia
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Proteínas del Citoesqueleto / Neuropatía Axonal Gigante / Mutación Tipo de estudio: Observational_studies / Prognostic_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Neurogenetics Asunto de la revista: GENETICA / NEUROLOGIA Año: 2020 Tipo del documento: Article País de afiliación: Francia