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Corrigendum: Intrafamilial variability in SLC6A1-related neurodevelopmental disorders.
Kassabian, Benedetta; Fenger, Christina Dühring; Willems, Marjolaine; Aledo-Serrano, Angel; Linnankivi, Tarja; McDonnell, Pamela Pojomovsky; Lusk, Laina; Jepsen, Birgit Susanne; Bayat, Michael; Kattentidt-Mouravieva, Anja A; Vidal, Anna Abulí; Valero-Lopez, Gabriel; Alarcon-Martinez, Helena; Goodspeed, Kimberly; van Slegtenhorst, Marjon; Barakat, Tahsin Stefan; Møller, Rikke S; Johannesen, Katrine M; Rubboli, Guido.
Affiliation
  • Kassabian B; Department of Epilepsy Genetics and Precision Medicine, Danish Epilepsy Center, Member of the European Reference Network EpiCARE, Dianalund, Denmark.
  • Fenger CD; Neurology Unit, Department of Neuroscience, University of Padua, Padua, Italy.
  • Willems M; Department of Epilepsy Genetics and Precision Medicine, Danish Epilepsy Center, Member of the European Reference Network EpiCARE, Dianalund, Denmark.
  • Aledo-Serrano A; Amplexa Genetics, Odense, Denmark.
  • Linnankivi T; 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.
  • McDonnell PP; Epilepsy and Neurogenetics Program-Vithas Madrid La Milagrosa University Hospital, Vithas Hospital Group, Madrid, Spain.
  • Lusk L; Department of Pediatric Neurology, New Children's Hospital and Pediatric Research Center, Epilepsia Helsinki, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
  • Jepsen BS; Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, United States.
  • Bayat M; Department of Neurology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, United States.
  • Kattentidt-Mouravieva AA; Epilepsy Neurogenetics Initiative, Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, United States.
  • Vidal AA; Epilepsy Neurogenetics Initiative, Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, United States.
  • Valero-Lopez G; Pediatric Department, Danish Epilepsy Center, Dianalund, Denmark.
  • Alarcon-Martinez H; Department of Neurology and Center for Rare Diseases, Aarhus University Hospital, Aarhus, Denmark.
  • Goodspeed K; Stichting Zuidwester, Middelharnis, Netherlands.
  • van Slegtenhorst M; Department of Clinical and Molecular Genetics, University Hospital Vall d'Hebron and Medicine Genetics Group Vall d'Hebron Research Institute (VHIR), Barcelona, Spain.
  • Barakat TS; Neurology Department, Virgen de la Arrixaca University Hospital, Murcia, Spain.
  • Møller RS; Department of Pediatric Neurology, Virgen de la Arrixaca University Hospital, Murcia, Spain.
  • Johannesen KM; Department of Pediatrics, Division of Neurology, University of Texas Southwestern Medical Center, Dallas, TX, United States.
  • Rubboli G; Department of Neurology, University of Texas Southwestern Medical Center, Dallas, TX, United States.
Front Neurosci ; 17: 1270299, 2023.
Article in En | MEDLINE | ID: mdl-37638311
ABSTRACT
[This corrects the article DOI 10.3389/fnins.2023.1219262.].
Key words