Articles with "scn3b encoding" as a keyword



Biallelic Truncating Variants in SCN3B Encoding Nav Channel Subunit β3 Lead to Neurodevelopmental Phenotype with and without Epilepsy and Ataxia

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Published in 2025 at "Annals of Neurology"

DOI: 10.1002/ana.78014

Abstract: SCN3B encodes the β3 auxiliary subunit, essential for voltage‐gated Na+ (Nav) channel trafficking and gating. Although SCN3B has been associated with cardiac disorders, a link with neurodevelopmental disorders (NDD) has not been established. Using a… read more here.

Keywords: ataxia; biallelic truncating; truncating variants; scn3b encoding ... See more keywords