Fig. 1From: Clinical phenotype features and genetic etiologies of 38 children with progressive myoclonic epilepsyThe 11 family pedigrees of proband and other affected members. SMA-PME: spinal muscular atrophy-progressive myoclonic epilepsy; PME: progressive myoclonic epilepsy; DRPLA: dentatorubral-pallidoluysian atrophy; TPP1: lysosomal enzyme tripeptidy l peptidase; EEG: electroencephalogramBack to article page