SCN1A Channels a Wide Range of Epileptic Phenotypes: Report of Novel and Known Variants with Variable Presentations
Article in International Journal of Molecular Sciences (May 2024)
The most recent citing publications are shown below. View all 3 publications that cite this research output on Dimensions.
Prediction of molecular phenotypes for novel SCN1A variants from a Turkish genetic epilepsy syndromes cohort and report of two new patients with recessive Dravet syndrome
Article in Clinical and Translational Science (December 2023)
Exome data of developmental and epileptic encephalopathy patients reveals de novo and inherited pathologic variants in epilepsy-associated genes
Article in Seizure (June 2023)