QuickView for KCNC2;jsessionid=3D4D7746C6F752CE93DDD7660CDE2C41 (gene)

1. Novel KCNC2 variant associated with developmental and epileptic encephalopathy.
2. Investigation of novel de novo KCNC2 variants causing severe developmental and early-onset epileptic…
3. Spectrum of Phenotypic, Genetic, and Functional Characteristics in Patients With Epilepsy With KCNC2…
4. A recurrent de novo variant supports KCNC2 involvement in the pathogenesis of developmental and epil…
5. A de novo heterozygous mutation in KCNC2 gene implicated in severe developmental and epileptic encep…

There were no clinical trials for KCNC2;jsessionid=3D4D7746C6F752CE93DDD7660CDE2C41