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Dravet Syndrome (DS) is most often caused by heterozygous loss-of-function mutations in the voltage-gated sodium channel gene SCN1A (Nav1. 1). resulting in severe epilepsy and neurodevelopmental impairment thought to be cause by reduced interneuron excitability. However. https://www.ealisboa.com/great-save-TV-Transparent-Drip-Logo-Grip-Tape-great-pick/
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