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Benedetta Kassabian1,2Christina Dühring Fenger1,3Marjolaine Willems4Angel Aledo-Serrano5Tarja Linnankivi6Pamela Pojomovsky McDonnell7,8,9Laina Lusk9Birgit Susanne Jepsen10Michael Bayat11Anja A. Kattentidt-Mouravieva12Anna Abulí Vidal13Gabriel Valero-Lopez14Helena Alarcon-Martinez15Kimberly Goodspeed16,17Marjon van Slegtenhorst18Tahsin Stefan Barakat18,19,20Rikke S. Møller1,21Katrine M. Johannesen1,22
Guido Rubboli1,23*- 1Department of Epilepsy Genetics and Precision Medicine, Danish Epilepsy Center, Member of the European Reference Network EpiCARE, Dianalund, Denmark
- 2Neurology Unit, Department of Neuroscience, University of Padua, Padua, Italy
- 3Amplexa Genetics, Odense, Denmark
- 4Département Génétique Médicale, Maladies Rares et Médecine Personnalisée, Hôpital Arnaud de Villeneuve, CHU de Montpellier Institute for Neurosciences of Montpellier, Univ Montpellier, INSERM, Montpellier, France
- 5Epilepsy and Neurogenetics Program—Vithas Madrid La Milagrosa University Hospital, Vithas Hospital Group, Madrid, Spain
- 6Department of Pediatric Neurology, New Children's Hospital and Pediatric Research Center, Epilepsia Helsinki, Helsinki University Hospital and University of Helsinki, Helsinki, Finland
- 7Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, United States
- 8Department of Neurology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, United States
- 9Epilepsy Neurogenetics Initiative, Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, United States
- 10Pediatric Department, Danish Epilepsy Center, Dianalund, Denmark
- 11Department of Neurology and Center for Rare Diseases, Aarhus University Hospital, Aarhus, Denmark
- 12Stichting Zuidwester, Middelharnis, Netherlands
- 13Department of Clinical and Molecular Genetics, University Hospital Vall d'Hebron and Medicine Genetics Group Vall d'Hebron Research Institute (VHIR), Barcelona, Spain
- 14Neurology Department, Virgen de la Arrixaca University Hospital, Murcia, Spain
- 15Department of Pediatric Neurology, Virgen de la Arrixaca University Hospital, Murcia, Spain
- 16Department of Pediatrics, Division of Neurology, University of Texas Southwestern Medical Center, Dallas, TX, United States
- 17Department of Neurology, University of Texas Southwestern Medical Center, Dallas, TX, United States
- 18Department of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, Netherlands
- 19Discovery Unit, Department of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, Netherlands
- 20ENCORE Expertise Center for Neurodevelopmental Disorders, Erasmus MC University Medical Center, Rotterdam, Netherlands
- 21Institute of Regional Health Research, University of Southern Denmark, Odense, Denmark
- 22Department of Genetics, University Hospital of Copenhagen, Rigshospitalet, Copenhagen, Denmark
- 23Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark
A corrigendum on
Intrafamilial variability in SLC6A1-related neurodevelopmental disorders
by Kassabian, B., Fenger, C. D., Willems, M., Aledo-Serrano, A., Linnankivi, T., McDonnell, P. P., Lusk, L., Jepsen, B. S., Bayat, M., Kattentidt-Mouravieva, A. A., Vidal, A. A., Valero-Lopez, G., Alarcon-Martinez, H., Goodspeed, K., van Slegtenhorst, M., Barakat, T. S., Møller, R. S., Johannesen, K. M., and Rubboli, G. (2023). Front. Neurosci. 17:1219262. doi: 10.3389/fnins.2023.1219262
In the published article, there was an error in affiliation 12. Instead of “Genetic Department, Stichting Zuidwester, Middelharnis, Netherlands”, it should be “Stichting Zuidwester, Middelharnis, Netherlands.”
In the published article, an author name was incorrectly written as Anja Kattentidt. The correct spelling is Anja A. Kattentidt-Mouravieva.
The initials in author contributions should not be AK but AK-M.
The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.
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Keywords: SLC6A1, intrafamilial variability, epilepsy, neurodevelopmental disorders, intellectual disability
Citation: Kassabian B, Fenger CD, Willems M, Aledo-Serrano A, Linnankivi T, McDonnell PP, Lusk L, Jepsen BS, Bayat M, Kattentidt-Mouravieva AA, Vidal AA, Valero-Lopez G, Alarcon-Martinez H, Goodspeed K, van Slegtenhorst M, Barakat TS, Møller RS, Johannesen KM and Rubboli G (2023) Corrigendum: Intrafamilial variability in SLC6A1-related neurodevelopmental disorders. Front. Neurosci. 17:1270299. doi: 10.3389/fnins.2023.1270299
Received: 31 July 2023; Accepted: 01 August 2023;
Published: 11 August 2023.
Approved by:
Frontiers Editorial Office, Frontiers Media SA, SwitzerlandCopyright © 2023 Kassabian, Fenger, Willems, Aledo-Serrano, Linnankivi, McDonnell, Lusk, Jepsen, Bayat, Kattentidt-Mouravieva, Vidal, Valero-Lopez, Alarcon-Martinez, Goodspeed, van Slegtenhorst, Barakat, Møller, Johannesen and Rubboli. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Guido Rubboli, Z3VydUBmaWxhZGVsZmlhLmRr