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Subject:

Research Funding:

National Institute of Neurological Disorders and Stroke : NINDS

Research in the authors’ laboratories is supported by grants from the NIH (NS065187 to AE and ALG, NS046484 and NS066155 to AE, NS048336 to ALG), the McKnight Foundation (34653 to ALG), and the Epilepsy Foundation (AE).

Keywords:

  • GEFS
  • Dravet syndrome
  • Genetics
  • Knock-in mice
  • Knockout mice

Sodium channel SCN1A and epilepsy: mutations and mechanisms

Tools:

Journal Title:

Epilepsia

Volume:

Volume 51, Number 9

Publisher:

, Pages 1650-1658

Type of Work:

Article | Post-print: After Peer Review

Abstract:

Summary Mutations in a number of genes encoding voltage-gated sodium channels cause a variety of epilepsy syndromes in humans, including genetic (generalized) epilepsy with febrile seizures Plus (GEFS+) and Dravet syndrome (DS, severe myoclonic epilepsy of infancy). The vast majority of these mutations are in the SCN1A gene, and all are dominantly inherited. Most of the mutations that cause DS result in loss of function, whereas all of the known mutations that cause GEFS+ are missense, presumably altering channel activity. Family members with the same GEFS+ mutation often display a wide range of seizure types and severities, and at least part of this variability likely results from variation in other genes. Many different biophysical effects of SCN1A-GEFS+ mutations have been observed in heterologous expression systems, consistent with both gain and loss of channel activity. However, results from mouse models suggest that the primary effect of both GEFS+ and DS mutations is to decrease the activity of GABAergic inhibitory neurons. Decreased activity of the inhibitory circuitry is thus likely to be a major factor contributing to seizure generation in patients with GEFS+ and DS, and may be a general consequence of SCN1A mutations.

Copyright information:

Wiley Periodicals, Inc. © 2010 International League Against Epilepsy

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