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Published in 2019 at "eLife"
DOI: 10.7554/elife.46846
Abstract: Dravet Syndrome (DS) is a severe neurodevelopmental disorder caused by pathogenic loss of function variants in the gene SCN1A which encodes the voltage gated sodium (Na+) channel subunit Nav1.1. GABAergic interneurons expressing parvalbumin (PV-INs) and…
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Keywords:
vip ins;
scn1a mice;
dravet syndrome;
vasoactive intestinal ... See more keywords