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. 2022 Apr 25;22:222. doi: 10.1186/s12887-022-03246-w

Fig. 1.

Fig. 1

A 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 dyskinesia