Fig. 1From: Damaging novel mutations in PIGN cause developmental epileptic-dyskinetic encephalopathy: a case reportA Ictal electroencephalograms showing no abnormalities. B Photographs showing no obvious dysmorphic features at the age of 1 year. C The PIGN mutations. D Phylogenetic conservation of the R55 and R95 (highlighted in red). E Schematic of the PIGN gene showing the putatively PNKD-related exons. Abbreviation: PNKD, paroxysmal nonkinesigenic dyskinesiaBack to article page