Fig. 2From: Clinical phenotype features and genetic etiologies of 38 children with progressive myoclonic epilepsyThe gene testing results of 30 patients with established PME genes. PME: progressive myoclonic epilepsy; DRPLA: dentatorubral-pallidoluysian atrophy; SMA-PME: spinal muscular atrophy-progressive myoclonic epilepsy; NCL: neuronal ceroid lipofuscinosesBack to article page