Correction to: Genetics in Medicine 2021; https://doi.org/10.1038/s41436-021-01161-6; Article published online 08 April 2021
Due to a processing error, the presentation of the online graphical abstract was incorrect.
PHRC National Mosaique was given as a Consortium by mistake in the author group; they are not part of the author group.
The original article has been corrected.
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Authors and Affiliations
INSERM UMR1231, Bourgogne Franche-Comté University, Dijon, France
Virginie Carmignac, Paul Kuentz, Arthur Sorlin, Jean-Benoît Courcet, Yannis Duffourd, Martin Chevarin, Patrick Callier, Christel Thauvin, Christophe Philippe, Jean-Baptiste Rivière, Laurence Faivre & Pierre Vabres
MAGEC-Mosaïque Reference Center, Dijon University Hospital, Dijon, France
Virginie Carmignac & Pierre Vabres
Neuropaediatrics and Development Pathology Department, Trousseau Hospital, AP–HP, Paris, France
Cyril Mignot
Genetics Department and Reference Center for rare causes of Intellectual Disability, Pitié-Salpêtrière hospital, AP-HP, Paris, France
Cyril Mignot & Diana Rodriguez
Plateforme IBiSA de Microscopie Electronique, Anatomie et cytologie pathologique, Université et CHRU de Tours, Tours, France
Emmanuelle Blanchard
INSERM U1259 MAVIVH, Université et CHRU de Tours, Tours, France
Emmanuelle Blanchard
Fédération Hospitalo-Universitaire Médecine Translationnelle et Anomalies du Développement (TRANSLAD), Dijon-Burgundy University Hospital, Dijon, France
Paul Kuentz, Arthur Sorlin, Jean-Benoît Courcet, Yannis Duffourd, Patrick Callier, Christel Thauvin, Jean-Baptiste Rivière, Laurence Faivre & Pierre Vabres
Pathology department, Dijon-Burgundy University Hospital, Dijon, France
Marie-Hélène Aubriot-Lorton
The University of Cambridge Metabolic Research Laboratories, Institute of Metabolic Science, Cambridge, UK
Victoria E. R. Parker, Rachel G. Knox & Robert K. Semple
Pediatrics and Medical Genetics Department, Dijon-Bourgogne University Hospital, Dijon, France
Arthur Sorlin, Jean-Benoît Courcet & Véronique Darmency
Service d’Anatomie et Cytologie Pathologique, Necker-Enfants Malades Hospital, Paris, France
Sylvie Fraitag
Paediatric Dermatology, Great Ormond St Hospital for Children NHS Foundation Trust, London, UK
Satyamaanasa Polubothu & Veronica A. Kinsler
UCL GOS Institute of Child Health, London, UK
Satyamaanasa Polubothu, Melissa Riachi & Veronica A. Kinsler
Mosaicism and Precision Medicine laboratory, Francis Crick Institute, London, UK
Satyamaanasa Polubothu, Melissa Riachi & Veronica A. Kinsler
National Genotyping Center, Genomic Institute, CEA, Evry, France
Anne Boland, Robert Olaso, Marc Delepine & Jean-François Deleuze
Clinical Genetics department, Rennes University Hospital, Rennes, France
Chloé Quelin, Paul Rollier, Louise Goujon & Sylvie Odent
Genetics Department, AP-HP, Robert-Debré University Hospital, Paris, France
Sarah Grotto & Yline Capri
Medical Genetics Unit, CHU La Réunion, Saint-Pierre, France
Marie-Line Jacquemont
Clinical Genetics Department, Créteil Hospital, Créteil, France
Daniel Amram
Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, FHU-TRANSLAD, CHU Dijon Bourgogne University Hospital, Dijon, France
Martin Chevarin
Medical Genetic Department, Jeanne de Flandre Hospital, Lille, France
Catherine Vincent-Delorme
Dermatology department, Lille University Hospital, Lille, France
Benoît Catteau
Pediatric and Fetal Imaging Department, Hospices Civils de Lyon, Bron, France
Laurent Guibaud
Department of Paediatric Clinical Epileptology, Sleep Disorders and Functional Neurology, University Hospitals of Lyon (HCL), Lyon, France
Alexis Arzimanoglou
Brain Dynamics and Cognition (DYCOG) Team, Lyon Neuroscience Research Centre, Lyon, France
Alexis Arzimanoglou
Cytogenetics Department, Dijon University Hospital, Dijon, France
Malika Keddar & Patrick Callier
Medical genetics department, Pôle Femme et Enfant, Clermont-Ferrand University Hospital–Hôpital d’Estaing, Clermont-Ferrand, France
Catherine Sarret
Dermatology Department, Montpellier University Hospital, Montpellier, France
Didier Bessis
Medical Genetics Department, Montpellier University Hospital, Montpellier, France
David Geneviève
Centre de Référence Déficiences Intellectuelles de Causes Rares, Hôpital d’Enfants, Dijon, France
Christel Thauvin
Center for Cardiovascular Science, University of Edinburgh, Edinburgh, UK
Robert K. Semple
Centre de Référence Anomalies du Développement et Syndromes Malformatifs, Hôpital d’Enfants, Dijon, France
Laurence Faivre
- Virginie Carmignac
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- Cyril Mignot
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- Emmanuelle Blanchard
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Correspondence to Virginie Carmignac.
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Carmignac, V., Mignot, C., Blanchard, E. et al. Correction to: Clinical spectrum of MTOR-related hypomelanosis of Ito with neurodevelopmental abnormalities. Genet Med 23, 1585 (2021). https://doi.org/10.1038/s41436-021-01217-7
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DOI: https://doi.org/10.1038/s41436-021-01217-7
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