Fig. 1From: Clinical features of patients with paroxysmal kinesigenic dyskinesia, mutation screening of PRRT2 and the effects of morning draughts of oxcarbazepineChromatograms of the detected variants. a Sequence traces of familial PRRT2 mutation with forward and reverse sequences reveal the deletion of TCAC at position 604–607, b Sequence traces of PRRT2 mutation reveal the duplication of C at position 629, c Sequence traces of PRRT2 mutation reveal the duplication of C at position 649Back to article page