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Publisher Correction: Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans.
Gstrein, Thomas; Edwards, Andrew; Pristoupilová, Anna; Leca, Ines; Breuss, Martin; Pilat-Carotta, Sandra; Hansen, Andi H; Tripathy, Ratna; Traunbauer, Anna K; Hochstoeger, Tobias; Rosoklija, Gavril; Repic, Marco; Landler, Lukas; Stránecký, Viktor; Dürnberger, Gerhard; Keane, Thomas M; Zuber, Johannes; Adams, David J; Flint, Jonathan; Honzik, Tomas; Gut, Marta; Beltran, Sergi; Mechtler, Karl; Sherr, Elliott; Kmoch, Stanislav; Gut, Ivo; Keays, David A.
Afiliación
  • Gstrein T; Institute of Molecular Pathology (IMP), Vienna Biocentre (VBC), Vienna, Austria.
  • Edwards A; Wellcome Trust Center for Human Genetics (WTCHG), Oxford, UK.
  • Pristoupilová A; Institute of Inherited Metabolic Disorders, Charles University, Prague, Czech Republic.
  • Leca I; CNAG-CRG, Centre for Genomic Regulation (CRG), Barcelona Institute of Science and Technology (BIST), Barcelona, Spain.
  • Breuss M; Universitat Pompeu Fabra (UPF), Barcelona, Spain.
  • Pilat-Carotta S; Institute of Molecular Pathology (IMP), Vienna Biocentre (VBC), Vienna, Austria.
  • Hansen AH; Institute of Molecular Pathology (IMP), Vienna Biocentre (VBC), Vienna, Austria.
  • Tripathy R; Institute of Molecular Pathology (IMP), Vienna Biocentre (VBC), Vienna, Austria.
  • Traunbauer AK; Institute of Molecular Pathology (IMP), Vienna Biocentre (VBC), Vienna, Austria.
  • Hochstoeger T; Institute of Molecular Pathology (IMP), Vienna Biocentre (VBC), Vienna, Austria.
  • Rosoklija G; Institute of Molecular Pathology (IMP), Vienna Biocentre (VBC), Vienna, Austria.
  • Repic M; Institute of Molecular Pathology (IMP), Vienna Biocentre (VBC), Vienna, Austria.
  • Landler L; Institute of Molecular Pathology (IMP), Vienna Biocentre (VBC), Vienna, Austria.
  • Stránecký V; Institute for Molecular Biotechnology (IMBA), Vienna, Austria.
  • Dürnberger G; Institute of Molecular Pathology (IMP), Vienna Biocentre (VBC), Vienna, Austria.
  • Keane TM; Institute of Inherited Metabolic Disorders, Charles University, Prague, Czech Republic.
  • Zuber J; Institute of Molecular Pathology (IMP), Vienna Biocentre (VBC), Vienna, Austria.
  • Adams DJ; Wellcome Trust Sanger Institute, Hinxton, Cambridgeshire, UK.
  • Flint J; Institute of Molecular Pathology (IMP), Vienna Biocentre (VBC), Vienna, Austria.
  • Honzik T; Wellcome Trust Sanger Institute, Hinxton, Cambridgeshire, UK.
  • Gut M; Wellcome Trust Center for Human Genetics (WTCHG), Oxford, UK.
  • Beltran S; Department of Pediatrics and Adolescent Medicine, First Faculty of Medicine, Charles University, Prague, Czech Republic.
  • Mechtler K; CNAG-CRG, Centre for Genomic Regulation (CRG), Barcelona Institute of Science and Technology (BIST), Barcelona, Spain.
  • Sherr E; Universitat Pompeu Fabra (UPF), Barcelona, Spain.
  • Kmoch S; CNAG-CRG, Centre for Genomic Regulation (CRG), Barcelona Institute of Science and Technology (BIST), Barcelona, Spain.
  • Gut I; Universitat Pompeu Fabra (UPF), Barcelona, Spain.
  • Keays DA; Institute of Molecular Pathology (IMP), Vienna Biocentre (VBC), Vienna, Austria.
Nat Neurosci ; 21(8): 1139, 2018 Aug.
Article en En | MEDLINE | ID: mdl-29875394

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: Nat Neurosci Asunto de la revista: NEUROLOGIA Año: 2018 Tipo del documento: Article País de afiliación: Austria

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: Nat Neurosci Asunto de la revista: NEUROLOGIA Año: 2018 Tipo del documento: Article País de afiliación: Austria