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.
Author information
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
Search author on:PubMed Google Scholar
- Cyril Mignot
Search author on:PubMed Google Scholar
- Emmanuelle Blanchard
Search author on:PubMed Google Scholar
- Paul Kuentz
Search author on:PubMed Google Scholar
- Marie-Hélène Aubriot-Lorton
Search author on:PubMed Google Scholar
- Victoria E. R. Parker
Search author on:PubMed Google Scholar
- Arthur Sorlin
Search author on:PubMed Google Scholar
- Sylvie Fraitag
Search author on:PubMed Google Scholar
- Jean-Benoît Courcet
Search author on:PubMed Google Scholar
- Yannis Duffourd
Search author on:PubMed Google Scholar
- Diana Rodriguez
Search author on:PubMed Google Scholar
- Rachel G. Knox
Search author on:PubMed Google Scholar
- Satyamaanasa Polubothu
Search author on:PubMed Google Scholar
- Anne Boland
Search author on:PubMed Google Scholar
- Robert Olaso
Search author on:PubMed Google Scholar
- Marc Delepine
Search author on:PubMed Google Scholar
- Véronique Darmency
Search author on:PubMed Google Scholar
- Melissa Riachi
Search author on:PubMed Google Scholar
- Chloé Quelin
Search author on:PubMed Google Scholar
- Paul Rollier
Search author on:PubMed Google Scholar
- Louise Goujon
Search author on:PubMed Google Scholar
- Sarah Grotto
Search author on:PubMed Google Scholar
- Yline Capri
Search author on:PubMed Google Scholar
- Marie-Line Jacquemont
Search author on:PubMed Google Scholar
- Sylvie Odent
Search author on:PubMed Google Scholar
- Daniel Amram
Search author on:PubMed Google Scholar
- Martin Chevarin
Search author on:PubMed Google Scholar
- Catherine Vincent-Delorme
Search author on:PubMed Google Scholar
- Benoît Catteau
Search author on:PubMed Google Scholar
- Laurent Guibaud
Search author on:PubMed Google Scholar
- Alexis Arzimanoglou
Search author on:PubMed Google Scholar
- Malika Keddar
Search author on:PubMed Google Scholar
- Catherine Sarret
Search author on:PubMed Google Scholar
- Patrick Callier
Search author on:PubMed Google Scholar
- Didier Bessis
Search author on:PubMed Google Scholar
- David Geneviève
Search author on:PubMed Google Scholar
- Jean-François Deleuze
Search author on:PubMed Google Scholar
- Christel Thauvin
Search author on:PubMed Google Scholar
- Robert K. Semple
Search author on:PubMed Google Scholar
- Christophe Philippe
Search author on:PubMed Google Scholar
- Jean-Baptiste Rivière
Search author on:PubMed Google Scholar
- Veronica A. Kinsler
Search author on:PubMed Google Scholar
- Laurence Faivre
Search author on:PubMed Google Scholar
- Pierre Vabres
Search author on:PubMed Google Scholar
Corresponding author
Correspondence to Virginie Carmignac.
Rights and permissions
About this article
Cite this article
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
Published:
Issue date:
DOI: https://doi.org/10.1038/s41436-021-01217-7
Share this article
Anyone you share the following link with will be able to read this content:
Sorry, a shareable link is not currently available for this article.
Provided by the Springer Nature SharedIt content-sharing initiative
