Correction to: Nature Genetics https://doi.org/10.1038/s41588-019-0498-4, published online 30 September 2019.
In the version of this article initially published, support from the Wellcome Trust and NIHR to author Veronica A. Kinsler was not included in the Acknowledgements. The error has been corrected in the HTML and PDF versions of the article.
Author information
These authors contributed equally: Pierre Vabres, Arthur Sorlin, Stanislav S. Kholmanskikh.
These authors jointly supervised this work: Laurence Faivre, M. Elizabeth Ross, Jean-Baptiste Rivière.
Authors and Affiliations
Fédération Hospitalo-Universitaire Médecine Translationnelle et Anomalies du Développement, Centre Hospitalier Universitaire Dijon Bourgogne, Dijon, France
Pierre Vabres, Arthur Sorlin, Judith St-Onge, Yannis Duffourd, Paul Kuentz, Jean-Benoît Courcet, Philippine Garret, Julien Thevenon, Christel Thauvin, Laurence Faivre & Jean-Baptiste Rivière
UMR Inserm 1231 Génétique des Anomalies du Développement, Université Bourgogne Franche-Comté, Dijon, France
Pierre Vabres, Arthur Sorlin, Judith St-Onge, Yannis Duffourd, Paul Kuentz, Jean-Benoît Courcet, Virginie Carmignac, Philippine Garret, Julien Thevenon, Christel Thauvin, Laurence Faivre & Jean-Baptiste Rivière
Centre de Référence MAGEC, Service de Dermatologie, Centre Hospitalier Universitaire Dijon Bourgogne, Dijon, France
Pierre Vabres, Arthur Sorlin & Virginie Carmignac
Service de Pédiatrie 1 et de Génétique Médicale, Centre Hospitalier Universitaire Dijon Bourgogne, Dijon, France
Arthur Sorlin, Jean-Benoît Courcet, Julien Thevenon, Christel Thauvin & Laurence Faivre
Center for Neurogenetics, Feil Family Brain and Mind Research Institute, Weill Cornell Medicine, New York, NY, USA
Stanislav S. Kholmanskikh & M. Elizabeth Ross
Unité de Génétique Médicale et Oncogénétique, Centre Hospitalier Universitaire Amiens Picardie, Amiens, France
Bénédicte Demeer & Michèle Mathieu-Dramard
EA CHIMERE–7516, Université Picardie Jules Verne, Amiens, France
Bénédicte Demeer & Bernard Devauchelle
Child Health and Human Development Program, Research Institute of the McGill University Health Centre, Montreal, Quebec, Canada
Judith St-Onge, Geneviève Bernard & Jean-Baptiste Rivière
Génétique Biologique Histologie, Centre Hospitalier Régional Universitaire de Besançon, Besançon, France
Paul Kuentz
Département de Dermatologie, Centre Hospitalier Universitaire de Montpellier, Montpellier, France
Didier Bessis
Service de Génétique Clinique, Centre Hospitalier Universitaire Lille, Lille, France
Odile Boute
Service d’Ophtalmologie, Centre Hospitalier Universitaire Dijon Bourgogne, Dijon, France
Alain Bron
Service de Chirurgie Orthopédique et plastique Pédiatrique, Centre Hospitalier Universitaire de Montpellier, Montpellier, France
Guillaume Captier
Dermatology Office, Amiens, France
Esther Carmi
Département de Chirurgie Maxillo-Faciale et Stomatologie, Centre Hospitalier Universitaire Amiens Picardie, Amiens, France
Bernard Devauchelle
Département de Génétique Médicale, Maladies rares et Médecine Personnalisée, Centre Hospitalier Universitaire de Montpellier, Montpellier, France
David Geneviève
Départment de Radiologie, Centre Hospitalier Universitaire Amiens Picardie, Amiens, France
Catherine Gondry-Jouet
Service d’Imagerie Pédiatrique et Fœtale, Hôpital Femme-Mère-Enfant Louis Pradel, Hospices Civils de Lyon, Bron, France
Laurent Guibaud
Service d’Odontologie-Stomatologie, Centre Hospitalier Universitaire Dijon Bourgogne, Dijon, France
Arnaud Lafon
Center for Integrative Brain Research, Seattle Children’s Research Institute, Seattle, WA, USA
William B. Dobyns
Departments of Neurology and Neurosurgery, and Pediatrics McGill University, Montreal, Quebec, Canada
Geneviève Bernard
Department of Medical Genetics, Montreal Children’s Hospital, McGill University Health Centre, Montreal, Quebec, Canada
Geneviève Bernard
Institute of Child Health, University College London, London, UK
Satyamaanasa Polubothu, Francesca Faravelli & Veronica A. Kinsler
Department of Human Genetics, Faculty of Medicine, McGill University, Montreal, Quebec, Canada
Jean-Baptiste Rivière
- Pierre Vabres
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Corresponding authors
Correspondence to Pierre Vabres or Jean-Baptiste Rivière.
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Vabres, P., Sorlin, A., Kholmanskikh, S.S. et al. Author Correction: Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome. Nat Genet 52, 353 (2020). https://doi.org/10.1038/s41588-019-0565-x
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DOI: https://doi.org/10.1038/s41588-019-0565-x
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