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Early developmental alterations of CA1 pyramidal cells in Dravet syndrome

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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.chiggate.com/queen-bee-female-honey-enhancements-cheap/
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