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EGR2 mutation enhances phenotype spectrum of Dejerine-Sottas syndrome.
Gargaun, Elena; Seferian, Andreea Mihaela; Cardas, Ruxandra; Le Moing, Anne-Gaelle; Delanoe, Catherine; Nectoux, Juliette; Nelson, Isabelle; Bonne, Gisèle; Bihoreau, Marie-Thérèse; Deleuze, Jean-François; Boland, Anne; Masson, Cécile; Servais, Laurent; Gidaro, Teresa.
Afiliación
  • Gargaun E; I-Motion, Pediatric Platform of Clinical Trials, Trousseau Hospital, Paris, France.
  • Seferian AM; I-Motion, Pediatric Platform of Clinical Trials, Trousseau Hospital, Paris, France.
  • Cardas R; I-Motion, Pediatric Platform of Clinical Trials, Trousseau Hospital, Paris, France.
  • Le Moing AG; I-Motion, Pediatric Platform of Clinical Trials, Trousseau Hospital, Paris, France.
  • Delanoe C; Neurological Function Test EMG/EEG Robert Debré Hospital, Paris, France.
  • Nectoux J; Molecular Genetics and Biochemistry Unit, HUPC Cochin Hospital, Paris, France.
  • Nelson I; Sorbonne University, UPMC Paris 06, INSERM UMRS974, CNRS FRE3617, Center for Research in Myology, 75013, Paris, France.
  • Bonne G; Sorbonne University, UPMC Paris 06, INSERM UMRS974, CNRS FRE3617, Center for Research in Myology, 75013, Paris, France.
  • Bihoreau MT; National Center of Genotyping, Institute of Genomics, CEA, Evry, France.
  • Deleuze JF; National Center of Genotyping, Institute of Genomics, CEA, Evry, France.
  • Boland A; National Center of Genotyping, Institute of Genomics, CEA, Evry, France.
  • Masson C; Bioinformatic Platform, Imagine Institute, Sorbonne University, Paris-Descartes, Paris, France.
  • Servais L; I-Motion, Pediatric Platform of Clinical Trials, Trousseau Hospital, Paris, France.
  • Gidaro T; I-Motion, Pediatric Platform of Clinical Trials, Trousseau Hospital, Paris, France. t.gidaro@institut-myologie.org.
J Neurol ; 263(7): 1456-8, 2016 Jul.
Article en En | MEDLINE | ID: mdl-27159987
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neuropatía Hereditaria Motora y Sensorial / Proteína 2 de la Respuesta de Crecimiento Precoz / Mutación Límite: Child, preschool / Female / Humans Idioma: En Revista: J Neurol Año: 2016 Tipo del documento: Article País de afiliación: Francia
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neuropatía Hereditaria Motora y Sensorial / Proteína 2 de la Respuesta de Crecimiento Precoz / Mutación Límite: Child, preschool / Female / Humans Idioma: En Revista: J Neurol Año: 2016 Tipo del documento: Article País de afiliación: Francia