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Published in 2022 at "Brain Research"
DOI: 10.1016/j.brainres.2021.147743
Abstract: Dravet Syndrome (DS) is a severe developmental and epileptic encephalopathy typically caused by loss-of-function de novo mutations in the SCN1A gene which encodes the voltage-gated sodium channel isoform NaV1.1. Decreased NaV1.1 expression results in impaired…
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Keywords:
excitability;
targeted augmentation;
gene;
dravet syndrome ... See more keywords