Correction to: Clinical spectrum of MTOR-related hypomelanosis of Ito with neurodevelopmental abnormalities

Affiliations

• ¹ INSERM UMR1231, Bourgogne Franche-Comté University, Dijon, France. [email protected].
• ² MAGEC-Mosaïque Reference Center, Dijon University Hospital, Dijon, France. [email protected].
• ³ Neuropaediatrics and Development Pathology Department, Trousseau Hospital, AP-HP, Paris, France.
• ⁴ Genetics Department and Reference Center for rare causes of Intellectual Disability, Pitié-Salpêtrière hospital, AP-HP, Paris, France.
• ⁵ Plateforme IBiSA de Microscopie Electronique, Anatomie et cytologie pathologique, Université et CHRU de Tours, Tours, France.
• ⁶ INSERM U1259 MAVIVH, Université et CHRU de Tours, Tours, France.
• ⁷ INSERM UMR1231, Bourgogne Franche-Comté University, Dijon, France.
• ⁸ Fédération Hospitalo-Universitaire Médecine Translationnelle et Anomalies du Développement (TRANSLAD), Dijon-Burgundy University Hospital, Dijon, France.
• ⁹ Pathology department, Dijon-Burgundy University Hospital, Dijon, France.
• ¹⁰ The University of Cambridge Metabolic Research Laboratories, Institute of Metabolic Science, Cambridge, UK.
• ¹¹ Pediatrics and Medical Genetics Department, Dijon-Bourgogne University Hospital, Dijon, France.
• ¹² Service d'Anatomie et Cytologie Pathologique, Necker-Enfants Malades Hospital, Paris, France.
• ¹³ Paediatric Dermatology, Great Ormond St Hospital for Children NHS Foundation Trust, London, UK.
• ¹⁴ UCL GOS Institute of Child Health, London, UK.
• ¹⁵ Mosaicism and Precision Medicine laboratory, Francis Crick Institute, London, UK.
• ¹⁶ National Genotyping Center, Genomic Institute, CEA, Evry, France.
• ¹⁷ Clinical Genetics department, Rennes University Hospital, Rennes, France.
• ¹⁸ Genetics Department, AP-HP, Robert-Debré University Hospital, Paris, France.
• ¹⁹ Medical Genetics Unit, CHU La Réunion, Saint-Pierre, France.
• ²⁰ Clinical Genetics Department, Créteil Hospital, Créteil, France.
• ²¹ Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, FHU-TRANSLAD, CHU Dijon Bourgogne University Hospital, Dijon, France.
• ²² Medical Genetic Department, Jeanne de Flandre Hospital, Lille, France.
• ²³ Dermatology department, Lille University Hospital, Lille, France.
• ²⁴ Pediatric and Fetal Imaging Department, Hospices Civils de Lyon, Bron, France.
• ²⁵ Department of Paediatric Clinical Epileptology, Sleep Disorders and Functional Neurology, University Hospitals of Lyon (HCL), Lyon, France.
• ²⁶ Brain Dynamics and Cognition (DYCOG) Team, Lyon Neuroscience Research Centre, Lyon, France.
• ²⁷ Cytogenetics Department, Dijon University Hospital, Dijon, France.
• ²⁸ Medical genetics department, Pôle Femme et Enfant, Clermont-Ferrand University Hospital-Hôpital d'Estaing, Clermont-Ferrand, France.
• ²⁹ Dermatology Department, Montpellier University Hospital, Montpellier, France.
• ³⁰ Medical Genetics Department, Montpellier University Hospital, Montpellier, France.
• ³¹ Centre de Référence Déficiences Intellectuelles de Causes Rares, Hôpital d'Enfants, Dijon, France.
• ³² Center for Cardiovascular Science, University of Edinburgh, Edinburgh, UK.
• ³³ Centre de Référence Anomalies du Développement et Syndromes Malformatifs, Hôpital d'Enfants, Dijon, France.
• ³⁴ MAGEC-Mosaïque Reference Center, Dijon University Hospital, Dijon, France.