Correction to: Genetics in Medicine https://doi.org/10.1038/s41436-018-0268-1; published online 12 September 2018
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Authors and Affiliations
INSERM, U 1127, CNRS UMR 7225, Sorbonne Universites, UPMC Univ Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle epiniere, ICM, Paris, France
Cyril Mignot MD, PhD, Caroline Nava MD, PhD & Christel Depienne PhD
APHP, Hôpital Pitie-Salpetriere, Departement de Genetique et de Cytogenetique; Centre de Reference Deficience Intellectuelle de Causes Rares, GRC UPMC «Deficience Intellectuelle et Autisme», Paris, France
Cyril Mignot MD, PhD, Julien Buratti MS, Caroline Nava MD, PhD, Pauline Marzin MD, Boris Keren MD, PhD & Delphine Héron MD
European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK
Aoife C. McMahon PhD, Claire Davidson PhD, Fiona Cunningham PhD & Joannella Morales PhD
APHP, Reference Centre for Rare Epilepsies, Necker-Enfants Malades Hospital, Imagine Institute, Paris Descartes University, Paris, France
Claire Bar MD & Rima Nabbout MD, PhD
INSERM U1163, Imagine Institute, Paris, France
Claire Bar MD, Giulia Barcia MD, PhD, Claude Besmond PhD, Laurence Hubert MS, Arnold Munnich MD, PhD & Rima Nabbout MD, PhD
Paris Descartes University, Paris, France
Claire Bar MD, Giulia Barcia MD, PhD, Claude Besmond PhD, Laurence Hubert MS, Arnold Munnich MD, PhD & Rima Nabbout MD, PhD
Division of Medical Genetics, Department of Pediatrics, CHU Sainte-Justine and University of Montreal, Montreal, QC, Canada
Philippe M. Campeau MD, Julie Gauthier PhD, Fadi F. Hamdan PhD, Jacques L. Michaud MD & Ivan Shelihan MD
CHU La Reunion–Groupe Hospitalier Sud Reunion, La Reunion, France
Marie-Line Jacquemont MD & Marilyn Tallot MD
APHM, Hôpital d’Enfants de La Timone, Service de Neurologie Pediatrique, centre de reference deficiences intellectuelles de cause rare, Marseille, France
Mathieu Milh MD, PhD
Aix Marseille University, INSERM, MMG, UMR-S 1251, Faculte de medecine, Marseille, France
Mathieu Milh MD, PhD & Laurent Villard PhD
Service de Genetique, Centre de Reference Anomalies du Developpement, Hospices Civils de Lyon, Bron, France
Patrick Edery MD, PhD, Audrey Putoux MD & Gaetan Lesca MD, PhD
INSERM U1028, CNRS UMR5292, Centre de Recherche en Neurosciences de Lyon, GENDEV Team, Universite Claude Bernard Lyon 1, Bron, France
Patrick Edery MD, PhD, Audrey Putoux MD & Gaetan Lesca MD, PhD
Claude Bernard Lyon I University, Lyon, France
Patrick Edery MD, PhD, Audrey Putoux MD & Gaetan Lesca MD, PhD
APHP, Service de genetique medicale, Necker- Enfants Malades Hospital, Imagine Institute, Paris Descartes University, Paris, France
Giulia Barcia MD, PhD, Stéphanie Gobin-Limballe PhD & Arnold Munnich MD, PhD
APHP, Unite fonctionnelle de Neurologie, Necker-Enfants Malades Hospital, Imagine Institute, Paris Descartes University, Paris, France
Christine Barnerias MD
APHP, Laboratoire de Genetique et Biologie Moleculaires, Hôpital Cochin, HUPC, Paris, France
Thierry Bienvenu PhD
Universite Paris Descartes Paris, Institut de Psychiatrie et de Neurosciences de Paris, Inserm U894, Paris, France
Thierry Bienvenu PhD
FHU-TRANSLAD, Universite de Bourgogne/CHU Dijon, Dijon, France
Ange-Line Bruel PhD & Daphné Lehalle MD
INSERM UMR 1231 GAD team, Genetics of Developmental disorders, Universite de Bourgogne-Franche Comte, Dijon, France
Ange-Line Bruel PhD
Division of Neurology, Department of Paediatrics, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada
Ledia Brunga MD, Elizabeth J. Donner MD & Berge A. Minassian MD
Department of Pediatric Neurology, University Hospital and University of Antwerp, Antwerp, Belgium
Berten Ceulemans MD, PhD
Departement de Genetique Medicale, Maladies rares et Medecine Personnalisee, CHU de Montpellier, Montpellier, France
Christine Coubes MD & David Geneviève MD, PhD
Division of Neurology, Children’s Hospital of Philadelphia, Philadelphia, PA, USA
Ana G. Cristancho MD, PhD, Ethan M. Goldberg MD, PhD, Xilma R. Ortiz-Gonzalez MD, PhD, Alyssa R. Rosen MD, Ingo Helbig MD & Katherine L. Helbig MS
Centre de Genetique Chromosomique, Hôpital St-Vincent-de-Paul, GHICL, Lille, France
Marie-Bertille Dehouck MD & Bénédicte Duban-Bedu MD
CHU Rennes, Service de Genetique Moleculaire et Genomique, Rennes, France
Christèle Dubourg PhD & Rikke S. Møller PhD
Danish Epilepsy Centre Filadelfia, Dianalund, Denmark
Elena Gardella MD, PhD, Dragan Marjanovic MD & Rikke S. Møller PhD
Institute for Regional Health Services, University of Southern Denmark, Odense, Denmark
Elena Gardella MD, PhD
INSERM, U1183, Montpellier, France
David Geneviève MD, PhD
Stichting Epilepsie Instellingen Nederland, SEIN, Zwolle, The Netherlands
Eveline Hagebeuk MD, PhD
Department of Biology and Medical Genetics, Charles University 2nd Faculty of Medicine and University Hospital Motol, Prague, Czech Republic
Miroslava Hančárová PhD, Darina Prchalová PhD & Emílie Vyhnálková MD
APHP, University Hospital of Paris ïle-de-France ouest, Raymond Poincare Hospital, Garches, France
Christine Ioos MD
Department of Clinical Diagnostics, Ambry Genetics, Aliso Viejo, CA, USA
Shoji Ichikawa PhD
Centre for Medical Genetics Ghent, Ghent University Hospital, C. Heymanslaan 10, Ghent, Belgium
Sandra Janssens MD, PhD
Service de Genetique Medicale, Hôpital Chubert, Vannes, France
Hubert Journel MD
APHP, Department of Clinical Neurophysiology, Necker-Enfants Malades Hospital, Paris, France
Anna Kaminska MD
Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands
Marije Koopmans MD, PhD, Marleen E. H. Simon MD, Jasper J. van der Smagt MD, Marjan van Kempen PhD, Bobby Koeleman PhD & Nienke E. Verbeek MD, PhD
Departement de Genetique Medicale, APHM, Hopital d’Enfants de La Timone, Marseille, France
Caroline Lacoste PhD & Laurent Villard PhD
Child Neurology Department, 2nd Faculty of Medicine, Charles University and Motol Hospital, Prague, Czech Republic
Petra Laššuthová PhD & Katalin Štěrbová MD
Centre de Genetique Humaine, Institut de Pathologie et de Genetique, Gosselies, Belgium
Damien Lederer MD, PhD
Unite fonctionnelle de genetique clinique, Centre Hospitalier Intercommunal de Creteil, Creteil, France
Daphné Lehalle MD
APHP, Service de neurologie pediatrique, Hôpital Universitaire Bicetre, Le Kremlin-Bicetre, France
Julia Métreau MD
Department of Pediatrics, Albany Medical Center, Albany, NY, USA
Kathryn Miller MS & Natasha Shur MD
APHP, Hôpital Trousseau, service de neuropediatrie, Paris, France
Marie-Laure Moutard MD
Sorbonne Universite, GRC n°19, pathologies Congenitales du Cervelet-LeucoDystrophies, APHP, Hôpital Armand Trousseau, Paris, France
Marie-Laure Moutard MD
Division of Neuropediatrics, CHU Raymond Poincare (APHP), Garches, France
Jean-Marc Pinard MD
Service de Genetique Medicale, CLAD Ouest CHU Hôpital Sud, Rennes, France
Chloé Quelin MD
Unite de Genetique Medicale, Centre de Reference des Maladies rares du Developpement (AnD DI Rares), CHI Poissy–St Germain en Laye, Poissy, France
Joelle Roume MD
Departments of Pediatrics and Neurosciences, CHU Sainte-Justine and University of Montreal, Montreal, Canada
Elsa Rossignol MD
Institut de Genetique Medicale, CHRU Lille, Universite de Lille, Lille, France
Thomas Smol MD
Department of Genetics, Hôpital Universitaire des Enfants Reine Fabiola, ULB Center of Human Genetics, Universite Libre de Bruxelles, Brussels, Belgium
Catheline Vilain MD, PhD, Julie Soblet PhD & Guillaume Smits MD, PhD
Department of Genetics, Hôpital Erasme, ULB Center of Human Genetics, Universite Libre de Bruxelles, Brussels, Belgium
Catheline Vilain MD, PhD, Julie Soblet PhD & Guillaume Smits MD, PhD
Interuniversity Institute of Bioinformatics in Brussels, Universite Libre de Bruxelles, Brussels, Belgium
Catheline Vilain MD, PhD, Julie Soblet PhD & Guillaume Smits MD, PhD
Clinical Genomics & Predictive Medicine, Providence Medical Group, Dayton, WA, USA
Samuel P. Yang MD
Department of Metabolic Diseases, Wilhelmina Children’s Hospital, University Medical Center, Utrecht, The Netherlands
Peter M. van Hasselt MD, PhD
Neurogenetics Group, Center of Molecular Neurology, VIB, Antwerp, Belgium
Sarah Weckhuysen MD, PhD
Neurology Department, University Hospital Antwerp, Antwerp, Belgium
Sarah Weckhuysen MD, PhD
IGBMC, CNRS UMR 7104/INSERM U964/Universite de Strasbourg, Illkirch, France
Christel Depienne PhD
Institute of Human Genetics, University Hospital Essen, University of Duisburg-Essen, Essen, Germany
Christel Depienne PhD
- Cyril Mignot MD, PhD
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Corresponding authors
Correspondence to Cyril Mignot MD, PhD or Christel Depienne PhD.
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Mignot, C., McMahon, A.C., Bar, C. et al. Correction: IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients. Genet Med 21, 1897–1898 (2019). https://doi.org/10.1038/s41436-018-0327-7
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DOI: https://doi.org/10.1038/s41436-018-0327-7
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