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scn2a protein human
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A Novel Splicing SCN2A Mutation in an Adolescent With Low-Functioning Autism, Acute Dystonic Movemen…
Epilepsy-associated SCN2A (NaV1.2) variants exhibit diverse and complex functional properties.
A De Novo Missense Variant of SCN2A: Implications and Limitations for Understanding Clinical Phenoty…
Functional correlates of clinical phenotype and severity in recurrent SCN2A variants.
SCN2A-related epilepsy of infancy with migrating focal seizures: report of a variant with apparent g…
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