Title : Role of SCN2A c.56G/A Gene Polymorphism in Egyptian Children with Genetic Epilepsy with Febrile Seizure Plus.

Pub. Date : 2022

PMID : 34607551






1 Functional Relationships(s)
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1 In the last decade, various coding and noncoding sequence variations of voltage-gated sodium channels SCN2A have been identified in patients with seizures, implying their genetic base. Sodium sodium voltage-gated channel alpha subunit 2 Homo sapiens