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

Journal

Genetics in medicine : official journal of the American College of Medical Genetics
ISSN: 1530-0366
Titre abrégé: Genet Med
Pays: United States
ID NLM: 9815831

Informations de publication

Date de publication:
Jul 2019
Historique:
pubmed: 21 2 2019
medline: 21 2 2019
entrez: 21 2 2019
Statut: ppublish

Résumé

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.

Identifiants

DOI: 10.1038/s41436-019-0460-y PMID: 30783266 PMC: PMC7608131
pubmed: 30783266
doi: 10.1038/s41436-019-0460-y
pii: S1098-3600(21)01706-8
pmc: PMC7608131
doi:

Types de publication

Published Erratum

Langues

eng

Pagination

1667-1671

Commentaires et corrections

Type : ErratumFor

Auteurs

Juliette Piard (J)

Centre de Génétique Humaine, Université de Franche-Comté, CHU Besançon, Besançon, France.

Lara Hawkes (L)

Oxford Centre for Genomic Medicine, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.

Mathieu Milh (M)

Aix Marseille Univ, Inserm, MMG, Marseille, France.
Pediatric Neurology, La Timone Children's Hospital, AP-HM, Marseille, France.

Laurent Villard (L)

Aix Marseille Univ, Inserm, MMG, Marseille, France.
Medical Genetics, La Timone Children's Hospital, AP-HM, Marseille, France.

Renato Borgatti (R)

Neuropsychiatry and Neurorehabilitation Unit, Scientific Institute IRCCS Eugenio Medea, Bosisio Parini, Italy.

Romina Romaniello (R)

Neuropsychiatry and Neurorehabilitation Unit, Scientific Institute IRCCS Eugenio Medea, Bosisio Parini, Italy.

Melanie Fradin (M)

Service de Génétique, CLAD Ouest, CHU Rennes, Rennes, France.

Yline Capri (Y)

Département de Génétique, Hôpital Robert Debré, APHP Paris, Paris, France.

Delphine Héron (D)

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.

Marie-Christine Nougues (MC)

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.

Caroline Nava (C)

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.

Oana Tarta Arsene (OT)

Pediatric Neurology Clinic, "Alexandru Obregia" Clinical Psychiatry Hospital, "Carol Davila" University of Medicine, Bucharest, Romania.

Debbie Shears (D)

Oxford Centre for Genomic Medicine, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.

John Taylor (J)

Oxford Medical Genetics Laboratories, Oxford University Hospitals NHS Foundation Trust, Churchill Hospital, Oxford, UK.

Alistair Pagnamenta (A)

NIHR Oxford Biomedical Research Centre, Wellcome Centre for Human Genetics, University of Oxford, Oxford, UK.

Jenny C Taylor (JC)

NIHR Oxford Biomedical Research Centre, Wellcome Centre for Human Genetics, University of Oxford, Oxford, UK.

Yoshimi Sogawa (Y)

Division of Pediatric Neurology, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, PA, USA.

Diana Johnson (D)

Department of Clinical Genetics, Sheffield Children's NHS Trust, Sheffield, United Kingdom.

Helen Firth (H)

Department of Clinical Genetics, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
Wellcome Trust Sanger Institute, Wellcome Genome Campus, Hinxton, UK.

Pradeep Vasudevan (P)

Clinical Genetics Department, University Hospitals Leicester NHS Trust, Leicester, UK.

Gabriela Jones (G)

Clinical Genetics Department, University Hospitals Leicester NHS Trust, Leicester, UK.

Marie-Ange Nguyen-Morel (MA)

Service de Neurologie pédiatrique, Hopital Couple Enfant, CHU Grenoble Alpes, Grenoble, France.

Tiffany Busa (T)

Medical Genetics, La Timone Children's Hospital, AP-HM, Marseille, France.

Agathe Roubertie (A)

Département de Neuropédiatrie, Centre Hospitalier Universitaire de Montpellier, INSERM U 1051, Institut des Neurosciences de Montpellier, Montpellier, France.

Myrthe van den Born (M)

Department for Clinical Genetics, Erasmus MC, Rotterdam, Netherlands.

Elise Brischoux-Boucher (E)

Centre de Génétique Humaine, Université de Franche-Comté, CHU Besançon, Besançon, France.

Michel Koenig (M)

EA7402 Institut Universitaire de Recherche Clinique, and Laboratoire de Génétique Moléculaire, CHU and Université de Montpellier, Montpellier, France.

Cyril Mignot (C)

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.

Usha Kini (U)

Oxford Centre for Genomic Medicine, Oxford University Hospitals NHS Foundation Trust, Oxford, UK. usha.kini@ouh.nhs.uk.

Christophe Philippe (C)

Laboratoire de génétique, Innovations en diagnostic génomique des maladies rares, Plateau Technique de Biologie, CHU Dijon, Dijon, France.
INSERM 1231, LNC UMR1231 GAD, Burgundy University, Dijon, France.

Classifications MeSH