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Autor:
Michał Sobstyl, Nina Kożuch, Magdalena Iwaniuk-Gugała, Angelika Stapińska-Syniec, Magdalena Konopko, Paweł Jezierski
Publikováno v:
Epilepsy & Behavior Reports, Vol 24, Iss , Pp 100627- (2023)
Progressive myoclonic epilepsy (PME) is characterized by prominent myoclonus, generalized tonic-clonic seizures, and less often focal, tonic, or absence seizures. The KCNC1 mutation is responsible for specific clinical phenotype of PME which has been
Externí odkaz:
https://doaj.org/article/03ebd3659f624f84989d8c926f0bcfdb