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.

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.

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

Article Tools

* Image Usage & Resolution