SCN1A channelopathies: Navigating from genotype to neural circuit dysfunction
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DOI: 10.3389/fneur.2023.1173460
Abstract: The SCN1A gene is strongly associated with epilepsy and plays a central role for supporting cortical excitation-inhibition balance through the expression of NaV1.1 within inhibitory interneurons. The phenotype of SCN1A disorders has been conceptualized as… read more here.
Keywords: channelopathies navigating; dysfunction; scn1a channelopathies; scn1a ... See more keywords