Abstract
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.
Cite
CITATION STYLE
APA
Garcia-Sosa, R., & Laux, L. C. (2016). Phenotypes of Dravet Syndrome. Pediatric Neurology Briefs, 30(5), 28. https://doi.org/10.15844/pedneurbriefs-30-5-1
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