QuickView for SCN3A;jsessionid=920ECB42E64C14162267BDAB971CEAFA (gene)

1. De novo SCN3A missense variant associated with self-limiting generalized epilepsy with fever sensiti…
2. Identification of a novel variant p.Ser606Gly in SCN3A associated with childhood absence epilepsy.
3. Knockdown of rno_circRNA_009194 Improves Outcomes in Traumatic Brain Injury Rats through Inhibiting …
4. Slow recovery from the inactivation of voltage-gated sodium channel Nav1.3 in mouse taste receptor c…
5. SCN3A-Related Neurodevelopmental Disorder: A Spectrum of Epilepsy and Brain Malformation.

There were no clinical trials for SCN3A;jsessionid=920ECB42E64C14162267BDAB971CEAFA