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Sporadic and Familial Variants in NF1: An Explanation of the Wide Variability in Neurocognitive Phenotype?
Biotteau, Maëlle; Déjean, Sébastien; Lelong, Sandrine; Iannuzzi, Stéphanie; Faure-Marie, Nathalie; Castelnau, Pierre; Rivier, François; Lauwers-Cancès, Valérie; Baudou, Eloïse; Chaix, Yves.
Afiliação
  • Biotteau M; ToNIC, Toulouse NeuroImaging Center, University of Toulouse, Inserm, UPS, Toulouse, France.
  • Déjean S; Children's Hospital, Toulouse-Purpan University Hospital, Toulouse, France.
  • Lelong S; Institut de Mathématiques de Toulouse, UMR5219 Université de Toulouse, CNRS UPS, Toulouse, France.
  • Iannuzzi S; Children's Hospital, Toulouse-Purpan University Hospital, Toulouse, France.
  • Faure-Marie N; Children's Hospital, Toulouse-Purpan University Hospital, Toulouse, France.
  • Castelnau P; Children's Hospital, Toulouse-Purpan University Hospital, Toulouse, France.
  • Rivier F; UMR 1253, iBrain, University of Tours, INSERM, Tours, France.
  • Lauwers-Cancès V; Department of Medicine, University of Tours Francois Rabelais, Tours, France.
  • Baudou E; Pediatric Neurology, Clocheville Children's Hospital, Tours University Hospital, Tours, France.
  • Chaix Y; Department of Pediatric Neurology and Reference Center for Language Disabilities, CHU Montpellier, PhyMedExp, University of Montpellier, INSERM, CNRS, Montpellier, France.
Front Neurol ; 11: 368, 2020.
Article em En | MEDLINE | ID: mdl-32431664
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article
Texto completo
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PubMed Links
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article