Correction: IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients

Cyril Mignot; Aoife C McMahon; Claire Bar; Philippe M Campeau; Claire Davidson; Julien Buratti; Caroline Nava; Marie-Line Jacquemont; Marilyn Tallot; Mathieu Milh; Patrick Edery; Pauline Marzin; Giulia Barcia; Christine Barnerias; Claude Besmond; Thierry Bienvenu; Ange-Line Bruel; Ledia Brunga; Berten Ceulemans; Christine Coubes; Ana G Cristancho; Fiona Cunningham; Marie-Bertille Dehouck; Elizabeth J Donner; Bénédicte Duban-Bedu; Christèle Dubourg; Elena Gardella; Julie Gauthier; David Geneviève; Stéphanie Gobin-Limballe; Ethan M Goldberg; Eveline Hagebeuk; Fadi F Hamdan; Miroslava Hančárová; Laurence Hubert; Christine Ioos; Shoji Ichikawa; Sandra Janssens; Hubert Journel; Anna Kaminska; Boris Keren; Marije Koopmans; Caroline Lacoste; Petra Laššuthová; Damien Lederer; Daphné Lehalle; Dragan Marjanovic; Julia Métreau; Jacques L Michaud; Kathryn Miller; Berge A Minassian; Joannella Morales; Marie-Laure Moutard; Arnold Munnich; Xilma R Ortiz-Gonzalez; Jean-Marc Pinard; Darina Prchalová; Audrey Putoux; Chloé Quelin; Alyssa R Rosen; Joelle Roume; Elsa Rossignol; Marleen E H Simon; Thomas Smol; Natasha Shur; Ivan Shelihan; Katalin Štěrbová; Emílie Vyhnálková; Catheline Vilain; Julie Soblet; Guillaume Smits; Samuel P Yang; Jasper J van der Smagt; Peter M van Hasselt; Marjan van Kempen; Sarah Weckhuysen; Ingo Helbig; Laurent Villard; Delphine Héron; Bobby Koeleman; Rikke S Møller; Gaetan Lesca; Katherine L Helbig; Rima Nabbout; Nienke E Verbeek; Christel Depienne

doi:10.1038/s41436-018-0327-7

. 2018 Oct 2;21(8):1897–1898. doi: 10.1038/s41436-018-0327-7

Correction: IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients

Cyril Mignot ^1,^2,^✉, Aoife C McMahon ³, Claire Bar ^4,^5,⁶, Philippe M Campeau ⁷, Claire Davidson ³, Julien Buratti ², Caroline Nava ^1,², Marie-Line Jacquemont ⁸, Marilyn Tallot ⁸, Mathieu Milh ^9,¹⁰, Patrick Edery ^11,^12,¹³, Pauline Marzin ², Giulia Barcia ^5,^6,¹⁴, Christine Barnerias ¹⁵, Claude Besmond ^5,⁶, Thierry Bienvenu ^16,¹⁷, Ange-Line Bruel ^18,¹⁹, Ledia Brunga ²⁰, Berten Ceulemans ²¹, Christine Coubes ²², Ana G Cristancho ²³, Fiona Cunningham ³, Marie-Bertille Dehouck ²⁴, Elizabeth J Donner ²⁰, Bénédicte Duban-Bedu ²⁴, Christèle Dubourg ²⁵, Elena Gardella ^26,²⁷, Julie Gauthier ⁷, David Geneviève ^22,²⁸, Stéphanie Gobin-Limballe ¹⁴, Ethan M Goldberg ²³, Eveline Hagebeuk ²⁹, Fadi F Hamdan ⁷, Miroslava Hančárová ³⁰, Laurence Hubert ^5,⁶, Christine Ioos ³¹, Shoji Ichikawa ³², Sandra Janssens ³³, Hubert Journel ³⁴, Anna Kaminska ³⁵, Boris Keren ², Marije Koopmans ³⁶, Caroline Lacoste ³⁷, Petra Laššuthová ³⁸, Damien Lederer ³⁹, Daphné Lehalle ^18,⁴⁰, Dragan Marjanovic ²⁶, Julia Métreau ⁴¹, Jacques L Michaud ⁷, Kathryn Miller ⁴², Berge A Minassian ²⁰, Joannella Morales ³, Marie-Laure Moutard ^43,⁴⁴, Arnold Munnich ^5,^6,¹⁴, Xilma R Ortiz-Gonzalez ²³, Jean-Marc Pinard ⁴⁵, Darina Prchalová ³⁰, Audrey Putoux ^11,^12,¹³, Chloé Quelin ⁴⁶, Alyssa R Rosen ²³, Joelle Roume ⁴⁷, Elsa Rossignol ⁴⁸, Marleen E H Simon ³⁶, Thomas Smol ⁴⁹, Natasha Shur ⁴², Ivan Shelihan ⁷, Katalin Štěrbová ³⁸, Emílie Vyhnálková ³⁰, Catheline Vilain ^50,^51,⁵², Julie Soblet ^50,^51,⁵², Guillaume Smits ^50,^51,⁵², Samuel P Yang ⁵³, Jasper J van der Smagt ³⁶, Peter M van Hasselt ⁵⁴, Marjan van Kempen ³⁶, Sarah Weckhuysen ^55,⁵⁶, Ingo Helbig ²³, Laurent Villard ^10,³⁷, Delphine Héron ², Bobby Koeleman ³⁶, Rikke S Møller ^25,²⁶, Gaetan Lesca ^11,^12,¹³, Katherine L Helbig ²³, Rima Nabbout ^4,^5,⁶, Nienke E Verbeek ³⁶, Christel Depienne ^1,^57,^58,^✉

¹INSERM, 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

²APHP, 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

³European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge UK

⁴APHP, Reference Centre for Rare Epilepsies, Necker-Enfants Malades Hospital, Imagine Institute, Paris Descartes University, Paris, France

⁵INSERM U1163, Imagine Institute, Paris, France

⁶Paris Descartes University, Paris, France

⁷Division of Medical Genetics, Department of Pediatrics, CHU Sainte-Justine and University of Montreal, Montreal, QC Canada

⁸CHU La Reunion–Groupe Hospitalier Sud Reunion, La Reunion, France

⁹APHM, Hôpital d’Enfants de La Timone, Service de Neurologie Pediatrique, centre de reference deficiences intellectuelles de cause rare, Marseille, France

¹⁰Aix Marseille University, INSERM, MMG, UMR-S 1251, Faculte de medecine, Marseille, France

¹¹Service de Genetique, Centre de Reference Anomalies du Developpement, Hospices Civils de Lyon, Bron, France

¹²INSERM U1028, CNRS UMR5292, Centre de Recherche en Neurosciences de Lyon, GENDEV Team, Universite Claude Bernard Lyon 1, Bron, France

¹³Claude Bernard Lyon I University, Lyon, France

¹⁴APHP, Service de genetique medicale, Necker- Enfants Malades Hospital, Imagine Institute, Paris Descartes University, Paris, France

¹⁵APHP, Unite fonctionnelle de Neurologie, Necker-Enfants Malades Hospital, Imagine Institute, Paris Descartes University, Paris, France

¹⁶APHP, Laboratoire de Genetique et Biologie Moleculaires, Hôpital Cochin, HUPC, Paris, France

¹⁷Universite Paris Descartes Paris, Institut de Psychiatrie et de Neurosciences de Paris, Inserm U894, Paris, France

¹⁸FHU-TRANSLAD, Universite de Bourgogne/CHU Dijon, Dijon, France

¹⁹INSERM UMR 1231 GAD team, Genetics of Developmental disorders, Universite de Bourgogne-Franche Comte, Dijon, France

²⁰Division of Neurology, Department of Paediatrics, The Hospital for Sick Children, University of Toronto, Toronto, ON Canada

²¹Department of Pediatric Neurology, University Hospital and University of Antwerp, Antwerp, Belgium

²²Departement de Genetique Medicale, Maladies rares et Medecine Personnalisee, CHU de Montpellier, Montpellier, France

²³Division of Neurology, Children’s Hospital of Philadelphia, Philadelphia, PA USA

²⁴Centre de Genetique Chromosomique, Hôpital St-Vincent-de-Paul, GHICL, Lille, France

²⁵CHU Rennes, Service de Genetique Moleculaire et Genomique, Rennes, France

²⁶Danish Epilepsy Centre Filadelfia, Dianalund, Denmark

²⁷Institute for Regional Health Services, University of Southern Denmark, Odense, Denmark

²⁸INSERM, U1183 Montpellier, France

²⁹Stichting Epilepsie Instellingen Nederland, SEIN, Zwolle, The Netherlands

³⁰Department of Biology and Medical Genetics, Charles University 2nd Faculty of Medicine and University Hospital Motol, Prague, Czech Republic

³¹APHP, University Hospital of Paris ïle-de-France ouest, Raymond Poincare Hospital, Garches, France

³²Department of Clinical Diagnostics, Ambry Genetics, Aliso Viejo, CA USA

³³Centre for Medical Genetics Ghent, Ghent University Hospital, C. Heymanslaan 10, Ghent, Belgium

³⁴Service de Genetique Medicale, Hôpital Chubert, Vannes, France

³⁵APHP, Department of Clinical Neurophysiology, Necker-Enfants Malades Hospital, Paris, France

³⁶Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands

³⁷Departement de Genetique Medicale, APHM, Hopital d’Enfants de La Timone, Marseille, France

³⁸Child Neurology Department, 2nd Faculty of Medicine, Charles University and Motol Hospital, Prague, Czech Republic

³⁹Centre de Genetique Humaine, Institut de Pathologie et de Genetique, Gosselies, Belgium

⁴⁰Unite fonctionnelle de genetique clinique, Centre Hospitalier Intercommunal de Creteil, Creteil, France

⁴¹APHP, Service de neurologie pediatrique, Hôpital Universitaire Bicetre, Le Kremlin-Bicetre, France

⁴²Department of Pediatrics, Albany Medical Center, Albany, NY USA

⁴³APHP, Hôpital Trousseau, service de neuropediatrie, Paris, France

⁴⁴Sorbonne Universite, GRC n°19, pathologies Congenitales du Cervelet-LeucoDystrophies, APHP, Hôpital Armand Trousseau, Paris, France

⁴⁵Division of Neuropediatrics, CHU Raymond Poincare (APHP), Garches, France

⁴⁶Service de Genetique Medicale, CLAD Ouest CHU Hôpital Sud, Rennes, France

⁴⁷Unite de Genetique Medicale, Centre de Reference des Maladies rares du Developpement (AnD DI Rares), CHI Poissy–St Germain en Laye, Poissy, France

⁴⁸Departments of Pediatrics and Neurosciences, CHU Sainte-Justine and University of Montreal, Montreal, Canada

⁴⁹Institut de Genetique Medicale, CHRU Lille, Universite de Lille, Lille, France

⁵⁰Department of Genetics, Hôpital Universitaire des Enfants Reine Fabiola, ULB Center of Human Genetics, Universite Libre de Bruxelles, Brussels, Belgium

⁵¹Department of Genetics, Hôpital Erasme, ULB Center of Human Genetics, Universite Libre de Bruxelles, Brussels, Belgium

⁵²Interuniversity Institute of Bioinformatics in Brussels, Universite Libre de Bruxelles, Brussels, Belgium

⁵³Clinical Genomics & Predictive Medicine, Providence Medical Group, Dayton, WA USA

⁵⁴Department of Metabolic Diseases, Wilhelmina Children’s Hospital, University Medical Center, Utrecht, The Netherlands

⁵⁵Neurogenetics Group, Center of Molecular Neurology, VIB, Antwerp, Belgium

⁵⁶Neurology Department, University Hospital Antwerp, Antwerp, Belgium

⁵⁷IGBMC, CNRS UMR 7104/INSERM U964/Universite de Strasbourg, Illkirch, France

⁵⁸Institute of Human Genetics, University Hospital Essen, University of Duisburg-Essen, Essen, Germany

^✉

Corresponding author.

PMCID: PMC7608434 PMID: 30279470

Correction to: Genetics in Medicine 10.1038/s41436-018-0268-1; published online 12 September 2018

This article was originally published under Nature Research’s License to Publish, but has now been made available under a CC BY 4.0 license. The PDF and HTML versions of the Article have been modified accordingly.

Contributor Information

Cyril Mignot, Email: cyril.mignot@aphp.fr.

Christel Depienne, Email: christel.depienne@uni-due.de.

PERMALINK

Correction: IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients

Cyril Mignot, MD, PhD

Aoife C McMahon, PhD

Claire Bar, MD

Philippe M Campeau, MD

Claire Davidson, PhD

Julien Buratti, MS

Caroline Nava, MD, PhD

Marie-Line Jacquemont, MD

Marilyn Tallot, MD

Mathieu Milh, MD, PhD

Patrick Edery, MD, PhD

Pauline Marzin, MD

Giulia Barcia, MD, PhD

Christine Barnerias, MD

Claude Besmond, PhD

Thierry Bienvenu, PhD

Ange-Line Bruel, PhD

Ledia Brunga, MD

Berten Ceulemans, MD, PhD

Christine Coubes, MD

Ana G Cristancho, MD, PhD

Fiona Cunningham, PhD

Marie-Bertille Dehouck, MD

Elizabeth J Donner, MD

Bénédicte Duban-Bedu, MD

Christèle Dubourg, PhD

Elena Gardella, MD, PhD

Julie Gauthier, PhD

David Geneviève, MD, PhD

Stéphanie Gobin-Limballe, PhD

Ethan M Goldberg, MD, PhD

Eveline Hagebeuk, MD, PhD

Fadi F Hamdan, PhD

Miroslava Hančárová, PhD

Laurence Hubert, MS

Christine Ioos, MD

Shoji Ichikawa, PhD

Sandra Janssens, MD, PhD

Hubert Journel, MD

Anna Kaminska, MD

Boris Keren, MD, PhD

Marije Koopmans, MD, PhD

Caroline Lacoste, PhD

Petra Laššuthová, PhD

Damien Lederer, MD, PhD

Daphné Lehalle, MD

Dragan Marjanovic, MD

Julia Métreau, MD

Jacques L Michaud, MD

Kathryn Miller, MS

Berge A Minassian, MD

Joannella Morales, PhD

Marie-Laure Moutard, MD

Arnold Munnich, MD, PhD

Xilma R Ortiz-Gonzalez, MD, PhD

Jean-Marc Pinard, MD

Darina Prchalová, PhD

Audrey Putoux, MD

Chloé Quelin, MD

Alyssa R Rosen, MD

Joelle Roume, MD

Elsa Rossignol, MD

Marleen E H Simon, MD

Thomas Smol, MD

Natasha Shur, MD

Ivan Shelihan, MD

Katalin Štěrbová, MD

Emílie Vyhnálková, MD

Catheline Vilain, MD, PhD

Julie Soblet, PhD

Guillaume Smits, MD, PhD

Samuel P Yang, MD

Jasper J van der Smagt, MD

Peter M van Hasselt, MD, PhD

Marjan van Kempen, PhD

Sarah Weckhuysen, MD, PhD

Ingo Helbig, MD

Laurent Villard, PhD