Pediatric Neurology Briefs (Aug 2016)

Phenotypes of Dravet Syndrome

  • Rebecca Garcia-Sosa,
  • Linda C. Laux

DOI
https://doi.org/10.15844/pedneurbriefs-30-5-1
Journal volume & issue
Vol. 30, no. 5

Abstract

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Researchers from the University of Washington in Seattle studied selective heterozygous and homozygous deletions of the voltage gated sodium channel (Nav1.1) in parvalbumin (PV) or somato-statin (SST) expressing interneurons.

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