Pediatric Neurology
Volume 30, Issue 4 , Pages 236-243, April 2004

Clinical correlations of mutations in the SCN1A gene: from febrile seizures to severe myoclonic epilepsy in infancy

  • Berten P.G.M Ceulemans, MD

      Affiliations

    • Department of Molecular Genetics, University of Antwerp, Antwerpen, Belgium
    • Department of Neurology-Child Neurology, University Hospital Antwerp (UZA), Antwerpen, Belgium
    • Epilepsy Center for Children and Youth, Pulderbos, Belgium
    • Corresponding Author InformationCommunications should be addressed to:Dr. Ceulemans; Epilepsy Genetics Project; Department of Molecular Genetics; University of Antwerp; Universiteitsplein 1; B-2610 Wilrijk; Belgium.
    • ,
  • Lieve R.F Claes, MSc

      Affiliations

    • Department of Molecular Genetics, University of Antwerp, Antwerpen, Belgium
    • ,
  • Lieven G Lagae, MD, PhD

      Affiliations

    • Epilepsy Center for Children and Youth, Pulderbos, Belgium
    • Department of Pediatric Neurology, University Hospital Gasthuisberg, Leuven, Belgium

Received 27 May 2003; accepted 20 October 2003.

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PII: S0887-8994(03)00579-4

doi:10.1016/j.pediatrneurol.2003.10.012

Pediatric Neurology
Volume 30, Issue 4 , Pages 236-243, April 2004

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