Refreshing results…
MED13 mutation: A novel cause of developmental and epileptic encephalopathy with infantile spasms
UploadDefining the phenotype of FHF1 developmental and epileptic encephalopathy
Download from api.wiley.comThe pharmacological management of Lennox-Gastaut syndrome and critical literature review
UploadMissing publications? Search for publications with a matching author name.