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Correction to: Clinical spectrum of MTOR-related hypomelanosis of Ito with neurodevelopmental abnormalities.
Carmignac, Virginie; Mignot, Cyril; Blanchard, Emmanuelle; Kuentz, Paul; Aubriot-Lorton, Marie-Hélène; Parker, Victoria E R; Sorlin, Arthur; Fraitag, Sylvie; Courcet, Jean-Benoît; Duffourd, Yannis; Rodriguez, Diana; Knox, Rachel G; Polubothu, Satyamaanasa; Boland, Anne; Olaso, Robert; Delepine, Marc; Darmency, Véronique; Riachi, Melissa; Quelin, Chloé; Rollier, Paul; Goujon, Louise; Grotto, Sarah; Capri, Yline; Jacquemont, Marie-Line; Odent, Sylvie; Amram, Daniel; Chevarin, Martin; Vincent-Delorme, Catherine; Catteau, Benoît; Guibaud, Laurent; Arzimanoglou, Alexis; Keddar, Malika; Sarret, Catherine; Callier, Patrick; Bessis, Didier; Geneviève, David; Deleuze, Jean-François; Thauvin, Christel; Semple, Robert K; Philippe, Christophe; Rivière, Jean-Baptiste; Kinsler, Veronica A; Faivre, Laurence; Vabres, Pierre.
Afiliação
  • Carmignac V; INSERM UMR1231, Bourgogne Franche-Comté University, Dijon, France. virginie.carmignac@chu-dijon.fr.
  • Mignot C; MAGEC-Mosaïque Reference Center, Dijon University Hospital, Dijon, France. virginie.carmignac@chu-dijon.fr.
  • Blanchard E; Neuropaediatrics and Development Pathology Department, Trousseau Hospital, AP-HP, Paris, France.
  • Kuentz P; Genetics Department and Reference Center for rare causes of Intellectual Disability, Pitié-Salpêtrière hospital, AP-HP, Paris, France.
  • Aubriot-Lorton MH; Plateforme IBiSA de Microscopie Electronique, Anatomie et cytologie pathologique, Université et CHRU de Tours, Tours, France.
  • Parker VER; INSERM U1259 MAVIVH, Université et CHRU de Tours, Tours, France.
  • Sorlin A; INSERM UMR1231, Bourgogne Franche-Comté University, Dijon, France.
  • Fraitag S; Fédération Hospitalo-Universitaire Médecine Translationnelle et Anomalies du Développement (TRANSLAD), Dijon-Burgundy University Hospital, Dijon, France.
  • Courcet JB; Pathology department, Dijon-Burgundy University Hospital, Dijon, France.
  • Duffourd Y; The University of Cambridge Metabolic Research Laboratories, Institute of Metabolic Science, Cambridge, UK.
  • Rodriguez D; INSERM UMR1231, Bourgogne Franche-Comté University, Dijon, France.
  • Knox RG; Fédération Hospitalo-Universitaire Médecine Translationnelle et Anomalies du Développement (TRANSLAD), Dijon-Burgundy University Hospital, Dijon, France.
  • Polubothu S; Pediatrics and Medical Genetics Department, Dijon-Bourgogne University Hospital, Dijon, France.
  • Boland A; Service d'Anatomie et Cytologie Pathologique, Necker-Enfants Malades Hospital, Paris, France.
  • Olaso R; INSERM UMR1231, Bourgogne Franche-Comté University, Dijon, France.
  • Delepine M; Fédération Hospitalo-Universitaire Médecine Translationnelle et Anomalies du Développement (TRANSLAD), Dijon-Burgundy University Hospital, Dijon, France.
  • Darmency V; Pediatrics and Medical Genetics Department, Dijon-Bourgogne University Hospital, Dijon, France.
  • Riachi M; INSERM UMR1231, Bourgogne Franche-Comté University, Dijon, France.
  • Quelin C; Fédération Hospitalo-Universitaire Médecine Translationnelle et Anomalies du Développement (TRANSLAD), Dijon-Burgundy University Hospital, Dijon, France.
  • Rollier P; Genetics Department and Reference Center for rare causes of Intellectual Disability, Pitié-Salpêtrière hospital, AP-HP, Paris, France.
  • Goujon L; The University of Cambridge Metabolic Research Laboratories, Institute of Metabolic Science, Cambridge, UK.
  • Grotto S; Paediatric Dermatology, Great Ormond St Hospital for Children NHS Foundation Trust, London, UK.
  • Capri Y; UCL GOS Institute of Child Health, London, UK.
  • Jacquemont ML; Mosaicism and Precision Medicine laboratory, Francis Crick Institute, London, UK.
  • Odent S; National Genotyping Center, Genomic Institute, CEA, Evry, France.
  • Amram D; National Genotyping Center, Genomic Institute, CEA, Evry, France.
  • Chevarin M; National Genotyping Center, Genomic Institute, CEA, Evry, France.
  • Vincent-Delorme C; Pediatrics and Medical Genetics Department, Dijon-Bourgogne University Hospital, Dijon, France.
  • Catteau B; UCL GOS Institute of Child Health, London, UK.
  • Guibaud L; Mosaicism and Precision Medicine laboratory, Francis Crick Institute, London, UK.
  • Arzimanoglou A; Clinical Genetics department, Rennes University Hospital, Rennes, France.
  • Keddar M; Clinical Genetics department, Rennes University Hospital, Rennes, France.
  • Sarret C; Clinical Genetics department, Rennes University Hospital, Rennes, France.
  • Callier P; Genetics Department, AP-HP, Robert-Debré University Hospital, Paris, France.
  • Bessis D; Genetics Department, AP-HP, Robert-Debré University Hospital, Paris, France.
  • Geneviève D; Medical Genetics Unit, CHU La Réunion, Saint-Pierre, France.
  • Deleuze JF; Clinical Genetics department, Rennes University Hospital, Rennes, France.
  • Thauvin C; Clinical Genetics Department, Créteil Hospital, Créteil, France.
  • Semple RK; INSERM UMR1231, Bourgogne Franche-Comté University, Dijon, France.
  • Philippe C; Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, FHU-TRANSLAD, CHU Dijon Bourgogne University Hospital, Dijon, France.
  • Rivière JB; Medical Genetic Department, Jeanne de Flandre Hospital, Lille, France.
  • Kinsler VA; Dermatology department, Lille University Hospital, Lille, France.
  • Faivre L; Pediatric and Fetal Imaging Department, Hospices Civils de Lyon, Bron, France.
  • Vabres P; Department of Paediatric Clinical Epileptology, Sleep Disorders and Functional Neurology, University Hospitals of Lyon (HCL), Lyon, France.
Genet Med ; 23(8): 1585, 2021 Aug.
Article em En | MEDLINE | ID: mdl-34257424
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
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PubMed Links
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article