Correction to: European Journal of Human Genetics https://doi.org/10.1038/s41431-024-01610-1, published online 27 April 2024
An author was not named.
The missing author is: “Annick Toutain”
Her affiliation is:
27 Service de Génétique, CHU de Tours, Tours, France.
28 UMR1253, iBrain, Inserm, University of Tours, Tours, France.
Author information
These authors contributed equally: Dana E. Layo-Carris, Emily E. Lubin, Annabel K. Sangree
Authors and Affiliations
Department of Human Genetics, Children’s Hospital of Philadelphia, Philadelphia, PA, USA
Dana E. Layo-Carris, Emily E. Lubin, Annabel K. Sangree, Kelly J. Clark, Emily L. Durham, Elizabeth M. Gonzalez, Sarina Smith, Rajesh Angireddy, Xiao Min Wang, Erin Weiss, Elizabeth J. K. Bhoj & Laura M. Bryant
Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA
Emily E. Lubin, Annabel K. Sangree, Kelly J. Clark, Elizabeth M. Gonzalez & Elizabeth J. K. Bhoj
Service de Génétique, CHU de Tours, Tours, France
Annick Toutain, Marie-Laure Vuillaume & Paul Gueguen
UMR1253, iBrain, Inserm, University of Tours, Tours, France
Annick Toutain, Marie-Laure Vuillaume & Paul Gueguen
Division of Clinical and Metabolic Genetics, Hospital for Sick Children, University of Toronto, Toronto, ON, Canada
Roberto Mendoza-Londono, Lucie Dupuis & Nadirah Damseh
Children’s Nebraska, University of Nebraska Medical Center, Omaha, NE, USA
Danita Velasco
Department of Clinical and Molecular Genetics and Rare Disease Unit Hospital Vall d’Hebron, Barcelona, Spain
Irene Valenzuela & Marta Codina-Solà
Medicine Genetics Group, Vall Hebron Research Institute, Barcelona, Spain
Irene Valenzuela & Marta Codina-Solà
Shodair Children’s Hospital, Helena, MT, USA
Catherine Ziats & Jaclyn Have
Greenwood Genetic Center, Greenwood, SC, USA
Katie Clarkson
UCL Great Ormond Street Institute of Child Health, London, UK
Dora Steel, Manju Kurian & Katy Barwick
Department of Clinical Genetics, Cook Children’s Hospital, Fort Worth, TX, USA
Diana Carrasco
Orlando Health, Arnold Palmer Hospital For Children, Orlando, FL, USA
Aditi I. Dagli
McMaster University Medical Centre, Hamilton, ON, Canada
M. J. M. Nowaczyk
Charles University Second Faculty of Medicine and University Hospital Motol, Prague, Czech Republic
Miroslava Hančárová, Šárka Bendová, Darina Prchalova & Zdeněk Sedláček
Charles University First Faculty of Medicine and General University Hospital, Prague, Czech Republic
Alica Baxová
Division of Genetics and Metabolism, Massachusetts General Hospital for Children, Boston, MA, USA
Catherine Bearce Nowak
Harvard Medical School, Boston, MA, USA
Jessica Douglas & Wendy K. Chung
Boston Children’s Hospital, Boston, MA, USA
Wendy K. Chung
University of Utah, Salt Lake City, UT, USA
Nicola Longo
Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany
Konrad Platzer, Chiara Klöckner & Ilona Krey
Institute of Human Genetics, Heinrich-Heine-University Düsseldorf, Medical Faculty, Düsseldorf, Germany
Luisa Averdunk & Dagmar Wieczorek
Institute of Human Genetics, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), 91054, Erlangen, Germany
Christiane Zweier & Andre Reis
Department of Human Genetics, Inselspital Bern, University of Bern, Bern, Switzerland
Christiane Zweier
University of Western Ontario, London, ON, Canada
Tugce Balci
Department of Genetics, University Medical Center, Utrecht, Netherlands
Marleen Simon, Hester Y. Kroes, Antje Wiesener & Georgia Vasileiou
Laboratory of Medical Genetics, St. Sophia’s Children’s Hospital, National and Kapodistrian University of Athens, Athens, Greece
Nikolaos M. Marinakis, Danai Veltra, Christalena Sofocleous, Konstantina Kosma & Joanne Traeger Synodinos
Second Department of Paediatrics, University of Athens, ‘P & A Kyriakou’ Children’s Hospital, Athens, Greece
Konstantinos A. Voudris
Laboratoire de Biologie Médicale Multi-Sites SeqOIA, Paris, France
Marie-Laure Vuillaume, Paul Gueguen & Nicolas Derive
Service de Génétique Médicale, CHU d’Angers, Angers, France
Estelle Colin & Clarisse Battault
University of Calgary, Calgary, AB, Canada
Billie Au
Victorian Clinical Genetics Services, Murdoch Children’s Research Institute, Parkville, VIC, Australia
Martin Delatycki & Lyndon Gallacher
Department of Paediatrics, University of Melbourne, Melbourne, VIC, Australia
Martin Delatycki & Lyndon Gallacher
Tasmanian Clinical Genetics Service, Tasmanian Health Service, Hobart, TAS, Australia
Mathew Wallis
School of Medicine and Menzies Institute for Medical Research, University of Tasmania, Hobart, TAS, Australia
Mathew Wallis
Applied and Translational Neurogenomics Group, VIB Center for Molecular Neurology, Antwerp, Belgium
Fatma Majdoub, Noor Smal & Sarah Weckhuysen
Applied and Translational Neurogenomics Group, Department of Biomedical Sciences, University of Antwerp, Antwerp, Belgium
Fatma Majdoub, Noor Smal & Sarah Weckhuysen
Medical Genetics Department, University Hedi Chaker Hospital of Sfax, Sfax, Tunisia
Fatma Majdoub
Department of Pediatric Neurology, University Hospital Antwerp, Antwerp, Belgium
Sarah Weckhuysen & An-Sofie Schoonjans
Translational Neurosciences, Faculty of Medicine and Health Science, University of Antwerp, Antwerp, Belgium
Sarah Weckhuysen
NEURO Research Centre of Excellence, University of Antwerp, Antwerp, Belgium
Sarah Weckhuysen
Department of Pediatrics, Duke University Hospital, Durham, NC, USA
An-Sofie Schoonjans, Marije Meuwissen & Benjamin T. Cocanougher
Center of Medical Genetics, Antwerp University Hospital/University of Antwerp, Edegem, Belgium
R. Frank Kooy & Marije Meuwissen
Division of Pediatric Neurology, Duke University Hospital, Durham, NC, USA
Kathryn Taylor & Carolyn E. Pizoli
Division of Medical Genetics, Duke University Hospital, Durham, NC, USA
Marie T. McDonald
DMG Children’s Rehabilitative Services, Phoenix, AZ, USA
Philip James
Department of Pediatrics, Baylor College of Medicine, San Antonio, TX, USA
Elizabeth R. Roeder, Rebecca Littlejohn & Stephanie Baskin
John T. Macdonald Foundation Department of Human Genetics, University of Miami Miller School of Medicine, Miami, FL, USA
Nicholas A. Borja & Willa Thorson
Genetics Department, Mary Bridge Children’s Hospital, Multicare Health System, Tacoma, WA, USA
Kristine King
Medical genetics department, Centre Hospitalier, Le Mans, France
Radka Stoeva
Department of Clinical Genetics, Leiden University Medical Center (LUMC), Leiden, The Netherlands
Manon Suerink & Esther Nibbeling
Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA
Stephanie Baskin
Service de Génétique médicale, Centre Labellisé Anomalies du Développement-Ouest Site, Poitiers, France
Gwenaël L. E. Guyader
Nemours Children’s Health, Wilmington, DE, USA
Julie Kaplan & Candace Muss
GeneDx, Gaithersburg, MD, USA
Deanna Alexis Carere
Steve and Cindy Rasmussen Institute for Genomic Medicine, Nationwide Children’s Hospital, Columbus, OH, USA
Laura M. Bryant
- Dana E. Layo-Carris
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- Emily E. Lubin
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- Annabel K. Sangree
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- Kelly J. Clark
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- Elizabeth M. Gonzalez
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Corresponding author
Correspondence to Elizabeth J. K. Bhoj.
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Layo-Carris, D.E., Lubin, E.E., Sangree, A.K. et al. Correction: Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals. Eur J Hum Genet 32, 1032 (2024). https://doi.org/10.1038/s41431-024-01659-y
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DOI: https://doi.org/10.1038/s41431-024-01659-y
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