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The voltage-dependent sodium channel protein type II subunit alpha (NaV1.2), encoded by the SCN2A gene, is a transmembrane glycoprotein that forms the pore of voltage-gated sodium channels in excitable cells such as neurons. It mediates voltage-dependent permeability to sodium ions, allowing rapid influx of Na+ during action potentials. Dysfunction of NaV1.2 due to genetic mutations is associated with a range of neurological disorders, including epilepsy and autism spectrum disorder.
Voltage-dependent sodium channel blockade
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