Correction to: Genetics in Medicine 2020; https://doi.org/10.1038/s41436-020-01020-w; published online 10 December 2020
Unfortunately, in the first sentence in the abstract, a spelling mistake was introduced during the production process after our proofreading. The wording was changed from “aims” to “aimsed.”
Heather M. McLaughlin was not listed among the authors.
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Authors and Affiliations
Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany
Chiara Klöckner, Bernt Popp, Johannes R. Lemke & Konrad Platzer
Institute of Biochemistry, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany
Heinrich Sticht
The Saxon Epilepsy Center Kleinwachau, Radeberg, Germany
Pia Zacher
Rare Disease Institute, Children’s National Hospital, Washington, DC, USA
Holly E. Babcock
Department of Child Neurology, Amsterdam University Medical Centers, Amsterdam, The Netherlands
Dewi P. Bakker
Institute of Child Health, University Collge London, London, UK
Katy Barwick, Manju A. Kurian & Amy McTague
Department of Pediatric Neurology and Developmental Medicine and LMU Center for Children with Medical Complexity, Dr. von Hauner Children’s Hospital, LMU - University Hospital, LudwigMaximilians-Universität, Munich, Germany
Michaela V. Bonfert
Neuromuscular and Neurogenetic Disorders of Childhood Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA
Carsten G. Bönnemann & Sandra Donkervoort
Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands
Eva H. Brilstra, Marie-José van den Boogaard, Koen L. I. van Gassen & Richard H. van Jaarsveld
Departments of Pediatrics and Medicine, Columbia University Medical Center, New York, NY, USA
Wendy K. Chung
Division of Cancer & Genetics, School of Medicine, Cardiff University, Wales, UK
Angus J. Clarke & Julian R. Sampson
Department of Pathology, University of California San Francisco, San Francisco, CA, USA
Patrick Devine & Jessica Van Ziffle
Rare Disease Institute, Division of Genetics and Metabolism, Children’s National Hospital, Washington, DC, USA
Jamie L. Fraser
Departments of Neurosciences and Pediatrics, University of California San Diego and Division of Neurology, Rady Children’s Hospital, San Diego, CA, USA
Jennifer Friedman
Rady Children’s Institute for Genomic Medicine, San Diego, CA, USA
Jennifer Friedman
Department of Genetic Services, Kaiser Permanente Washington, Seattle, WA, USA
Alyssa Gates & Kathleen A. Leppig
Service de Génétique Clinique, Hôpital Jeanne de Flandre, CHU Lille, Lille, France
Jamal Ghoumid
Yorkshire Clinical Genetics Service, Chapel Allerton Hospital, Leeds, UK
Emma Hobson
Department of Pediatrics, Division of Biochemical Diseases, University of British Columbia, Vancouver, Canada
Gabriella Horvath
GeneDx, Gaithersburg, MD, USA
Jennifer Keller-Ramey
APHP, Département de Génétique, Groupe Hospitalier Pitié Salpêtrière, Paris, France
Boris Keren
Department of Neurology, University of California San Francisco, San Francisco, CA, USA
Virgina Lee
Institute of Clinical Sciences, Skane University Hospital, Lund, Sweden
Johan Lundgren
Division of Medical Genetics, Department of Pediatrics, Duke University Medical Center, Durham, NC, USA
Marie T. McDonald, Vandana Shashi & Jennifer A. Sullivan
Invitae Corporation, San Francisco, CA, USA
Heather M. McLaughlin
Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, WA, USA
Heather C. Mefford
Département de Génétique, Centre de Référence Déficiences Intellectuelles de Causes Rares, Groupe Hospitalier Pitié Salpêtrière et Hôpital Trousseau, APHP, Sorbonne Université, Paris, France
Cyril Mignot
Division of Pediatric Neurology, Department of Pediatrics, Duke University Medical Center, Durham, NC, USA
Mohamad A. Mikati
Sorbonne University, Paris Brain Institute, Inserm U1127, CNRS UMR 7225, AP-HP, Pitié Salpêtrière Hospital, Department of Genetics, Paris, France
Caroline Nava
NIHR BioResource, Cambridge University Hospitals NHS Foundation Trust, Cambridge Biomedical Campus, Cambridge, UK
F. Lucy Raymond & Alba Sanchis-Juan
Department of Medical Genetics, Cambridge Institute for Medical Research, University of Cambridge, Cambridge, UK
F. Lucy Raymond
Department of Haematology, University of Cambridge, NHS Blood and Transplant Centre, Cambridge, UK
Alba Sanchis-Juan
Division of Medical Genetics, University of California, San Francisco, San Francisco, CA, USA
Joseph T. C. Shieh & Anne Slavotinek
Institute for Human Genetics, University of California, San Francisco, San Francisco, CA, USA
Joseph T. C. Shieh
Department of Pediatrics, Division of Genetics and Genomic Medicine, Washington University School of Medicine, St. Louis, MO, USA
Marwan Shinawi & Tomi L. Toler
Department of Women’s and Children’s Health Karolinska Institutet, Stockholm, Sweden
Tommy Stödberg
Institute for Genomic Medicine, Columbia University, New York, NY, USA
Nicholas Stong
Section of Genetics, Department of Pediatrics, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA
Ashley C. Taylor
Department of Clinical Genetics, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands
Saskia N. van der Crabben
University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA
Alexandrea F. Wadley
Institute of Neurogenomics, Helmholtz Zentrum Munich, Neuherberg, Germany
Matias Wagner
Department of Pediatrics, Division of Genetics, University of California, San Diego and Rady Children’s Hospital-San Diego, San Diego, CA, USA
Kristen Wigby
Amalia Children’s Hospital, Radboud University Nijmegen, Nijmegen, The Netherlands
Saskia B. Wortmann
University Childrens Hospital, Paracelsus Medical University, Salzburg, Austria
Saskia B. Wortmann
Section of Genetics and Metabolism, Department of Pediatrics, University of Arkansas for Medical Sciences, Little Rock, AR, USA
Yuri A. Zarate
Institute for Regional Health Services, University of Southern Denmark, Odense, Denmark
Rikke S. Møller
Department of Epilepsy Genetics and Personalized Medicine, Danish Epilepsy Centre Filadelfia, Dianalund, Denmark
Rikke S. Møller
- Chiara Klöckner
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- Heinrich Sticht
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- Pia Zacher
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- Bernt Popp
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- Michaela V. Bonfert
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- Patrick Devine
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- Jamie L. Fraser
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- Jennifer Friedman
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- Alyssa Gates
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- Jamal Ghoumid
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- Emma Hobson
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- Jennifer Keller-Ramey
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- Marie T. McDonald
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- Heather M. McLaughlin
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- Heather C. Mefford
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- Cyril Mignot
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- Mohamad A. Mikati
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- Caroline Nava
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- Vandana Shashi
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- Joseph T. C. Shieh
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- Marwan Shinawi
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- Anne Slavotinek
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- Tommy Stödberg
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- Nicholas Stong
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- Jennifer A. Sullivan
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- Ashley C. Taylor
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- Tomi L. Toler
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- Marie-José van den Boogaard
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- Konrad Platzer
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Consortia
Care4Rare Canada Consortium
Corresponding author
Correspondence to Konrad Platzer.
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Klöckner, C., Sticht, H., Zacher, P. et al. Correction to: De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathy. Genet Med 23, 796 (2021). https://doi.org/10.1038/s41436-020-01090-w
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DOI: https://doi.org/10.1038/s41436-020-01090-w
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