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

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.

PMID: 30783266
PMCID: PMC7608131
DOI: 10.1038/s41436-019-0460-y

Published Erratum

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

Juliette Piard et al. Genet Med. 2019 Jul.

. 2019 Jul;21(7):1667-1671.

doi: 10.1038/s41436-019-0460-y.

Authors

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.

PMID: 30783266
PMCID: PMC7608131
DOI: 10.1038/s41436-019-0460-y

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.

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Erratum for

The phenotypic spectrum of WWOX-related disorders: 20 additional cases of WOREE syndrome and review of the literature.
Piard J, Hawkes L, Milh M, Villard L, Borgatti R, Romaniello R, Fradin M, Capri Y, Héron D, Nougues MC, Nava C, Arsene OT, Shears D, Taylor J, Pagnamenta A, Taylor JC, Sogawa Y, Johnson D, Firth H, Vasudevan P, Jones G, Nguyen-Morel MA, Busa T, Roubertie A, van den Born M, Brischoux-Boucher E, Koenig M, Mignot C; DDD Study; Kini U, Philippe C. Piard J, et al. Genet Med. 2019 Jun;21(6):1308-1318. doi: 10.1038/s41436-018-0339-3. Epub 2018 Oct 25. Genet Med. 2019. PMID: 30356099 Free PMC article. Review.

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

Affiliations

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

Authors

Affiliations

Abstract

Erratum for

Publication types

LinkOut - more resources

Full Text Sources