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CORRECTION article

Front. Neurosci., 11 August 2023

Sec. Neurodevelopment

Volume 17 - 2023 | https://doi.org/10.3389/fnins.2023.1270299

Corrigendum: Intrafamilial variability in SLC6A1-related neurodevelopmental disorders

    BK

    Benedetta Kassabian 1,2

    CD

    Christina Dühring Fenger 1,3

    MW

    Marjolaine Willems 4

    AA

    Angel Aledo-Serrano 5

    TL

    Tarja Linnankivi 6

    PP

    Pamela Pojomovsky McDonnell 7,8,9

    LL

    Laina Lusk 9

    BS

    Birgit Susanne Jepsen 10

    MB

    Michael Bayat 11

    AA

    Anja A. Kattentidt-Mouravieva 12

    AA

    Anna Abulí Vidal 13

    GV

    Gabriel Valero-Lopez 14

    HA

    Helena Alarcon-Martinez 15

    KG

    Kimberly Goodspeed 16,17

    MV

    Marjon van Slegtenhorst 18

    TS

    Tahsin Stefan Barakat 18,19,20

    RS

    Rikke S. Møller 1,21

    KM

    Katrine M. Johannesen 1,22

    GR

    Guido Rubboli 1,23*

  • 1. Department of Epilepsy Genetics and Precision Medicine, Danish Epilepsy Center, Member of the European Reference Network EpiCARE, Dianalund, Denmark

  • 2. Neurology Unit, Department of Neuroscience, University of Padua, Padua, Italy

  • 3. Amplexa Genetics, Odense, Denmark

  • 4. Département Génétique Médicale, Maladies Rares et Médecine Personnalisée, Hôpital Arnaud de Villeneuve, CHU de Montpellier Institute for Neurosciences of Montpellier, Univ Montpellier, INSERM, Montpellier, France

  • 5. Epilepsy and Neurogenetics Program—Vithas Madrid La Milagrosa University Hospital, Vithas Hospital Group, Madrid, Spain

  • 6. Department of Pediatric Neurology, New Children's Hospital and Pediatric Research Center, Epilepsia Helsinki, Helsinki University Hospital and University of Helsinki, Helsinki, Finland

  • 7. Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, United States

  • 8. Department of Neurology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, United States

  • 9. Epilepsy Neurogenetics Initiative, Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, United States

  • 10. Pediatric Department, Danish Epilepsy Center, Dianalund, Denmark

  • 11. Department of Neurology and Center for Rare Diseases, Aarhus University Hospital, Aarhus, Denmark

  • 12. Stichting Zuidwester, Middelharnis, Netherlands

  • 13. Department of Clinical and Molecular Genetics, University Hospital Vall d'Hebron and Medicine Genetics Group Vall d'Hebron Research Institute (VHIR), Barcelona, Spain

  • 14. Neurology Department, Virgen de la Arrixaca University Hospital, Murcia, Spain

  • 15. Department of Pediatric Neurology, Virgen de la Arrixaca University Hospital, Murcia, Spain

  • 16. Department of Pediatrics, Division of Neurology, University of Texas Southwestern Medical Center, Dallas, TX, United States

  • 17. Department of Neurology, University of Texas Southwestern Medical Center, Dallas, TX, United States

  • 18. Department of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, Netherlands

  • 19. Discovery Unit, Department of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, Netherlands

  • 20. ENCORE Expertise Center for Neurodevelopmental Disorders, Erasmus MC University Medical Center, Rotterdam, Netherlands

  • 21. Institute of Regional Health Research, University of Southern Denmark, Odense, Denmark

  • 22. Department of Genetics, University Hospital of Copenhagen, Rigshospitalet, Copenhagen, Denmark

  • 23. Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark

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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.

Statements

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Summary

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, Switzerland

Volume

17 - 2023

Updates

Copyright

*Correspondence: Guido Rubboli

Disclaimer

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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