Correction: The phenotypic spectrum of WWOX-related disorders: 20 additional cases of WOREE syndrome and review of the literature

Juliette Piard; Lara Hawkes; Mathieu Milh; Laurent Villard; Renato Borgatti; Romina Romaniello; Melanie Fradin; Yline Capri; Delphine Héron; Marie-Christine Nougues; Caroline Nava; Oana Tarta Arsene; Debbie Shears; John Taylor; Alistair Pagnamenta; Jenny C Taylor; Yoshimi Sogawa; Diana Johnson; Helen Firth; Pradeep Vasudevan; Gabriela Jones; Marie-Ange Nguyen-Morel; Tiffany Busa; Agathe Roubertie; Myrthe van den Born; Elise Brischoux-Boucher; Michel Koenig; Cyril Mignot; DDD Study; Usha Kini; Christophe Philippe

doi:10.1038/s41436-019-0460-y

Correction: The phenotypic spectrum of WWOX-related disorders: 20 additional cases of WOREE syndrome and review of the literature

Genet Med. 2019 Jul;21(7):1667-1671. doi: 10.1038/s41436-019-0460-y.

Authors

Juliette Piard¹, Lara Hawkes², Mathieu Milh^{3

4}, Laurent Villard^{3

5}, Renato Borgatti⁶, Romina Romaniello⁶, Melanie Fradin⁷, Yline Capri⁸, Delphine Héron⁹, Marie-Christine Nougues¹⁰, Caroline Nava¹¹, Oana Tarta Arsene¹², Debbie Shears², John Taylor¹³, Alistair Pagnamenta¹⁴, Jenny C Taylor¹⁴, Yoshimi Sogawa¹⁵, Diana Johnson¹⁶, Helen Firth^{17

18}, Pradeep Vasudevan¹⁹, Gabriela Jones¹⁹, Marie-Ange Nguyen-Morel²⁰, Tiffany Busa⁵, Agathe Roubertie²¹, Myrthe van den Born²², Elise Brischoux-Boucher¹, Michel Koenig²³, Cyril Mignot⁹; DDD Study; Usha Kini²⁴, Christophe Philippe^{25

26}

Affiliations

¹ Centre de Génétique Humaine, Université de Franche-Comté, CHU Besançon, Besançon, France.
² Oxford Centre for Genomic Medicine, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
³ Aix Marseille Univ, Inserm, MMG, Marseille, France.
⁴ Pediatric Neurology, La Timone Children's Hospital, AP-HM, Marseille, France.
⁵ Medical Genetics, La Timone Children's Hospital, AP-HM, Marseille, France.
⁶ Neuropsychiatry and Neurorehabilitation Unit, Scientific Institute IRCCS Eugenio Medea, Bosisio Parini, Italy.
⁷ Service de Génétique, CLAD Ouest, CHU Rennes, Rennes, France.
⁸ Département de Génétique, Hôpital Robert Debré, APHP Paris, Paris, France.
⁹ APHP, Département de Génétique, Centre de Référence Déficiences Intellectuelles de Causes Rares, Groupe Hospitalier Pitié Salpêtrière et GHUEP Hôpital Trousseau, Sorbonne Université, GRC "Déficience Intellectuelle et Autisme", Paris, France.
¹⁰ Neuropédiatrie et Unité d'électrophysiologie clinique, Centre de Référence des Maladies Neuromusculaires de l'EST parisien et DHU I2B, Hôpital d'Enfants Armand Trousseau, Paris, France.
¹¹ Département de Génétique, Sorbonne Universités, Institut du Cerveau et de la Moelle épinière, ICM, Inserm U1127, CNRS UMR 7225, APHP, Hôpital de la Pitié Salpêtrière, Paris, France.
¹² Pediatric Neurology Clinic, "Alexandru Obregia" Clinical Psychiatry Hospital, "Carol Davila" University of Medicine, Bucharest, Romania.
¹³ Oxford Medical Genetics Laboratories, Oxford University Hospitals NHS Foundation Trust, Churchill Hospital, Oxford, UK.
¹⁴ NIHR Oxford Biomedical Research Centre, Wellcome Centre for Human Genetics, University of Oxford, Oxford, UK.
¹⁵ Division of Pediatric Neurology, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, PA, USA.
¹⁶ Department of Clinical Genetics, Sheffield Children's NHS Trust, Sheffield, United Kingdom.
¹⁷ Department of Clinical Genetics, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
¹⁸ Wellcome Trust Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
¹⁹ Clinical Genetics Department, University Hospitals Leicester NHS Trust, Leicester, UK.
²⁰ Service de Neurologie pédiatrique, Hopital Couple Enfant, CHU Grenoble Alpes, Grenoble, France.
²¹ Département de Neuropédiatrie, Centre Hospitalier Universitaire de Montpellier, INSERM U 1051, Institut des Neurosciences de Montpellier, Montpellier, France.
²² Department for Clinical Genetics, Erasmus MC, Rotterdam, Netherlands.
²³ EA7402 Institut Universitaire de Recherche Clinique, and Laboratoire de Génétique Moléculaire, CHU and Université de Montpellier, Montpellier, France.
²⁴ Oxford Centre for Genomic Medicine, Oxford University Hospitals NHS Foundation Trust, Oxford, UK. usha.kini@ouh.nhs.uk.
²⁵ Laboratoire de génétique, Innovations en diagnostic génomique des maladies rares, Plateau Technique de Biologie, CHU Dijon, Dijon, France.
²⁶ INSERM 1231, LNC UMR1231 GAD, Burgundy University, Dijon, France.

Abstract

The article has been corrected to account for one patient being investigated through genome sequencing rather than exome sequencing as originally published; thus amendments to the Abstract and Methods have been made as well as addition of the relevant authors and acknowledgment.

Publication types

Published Erratum