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Fig. 1 | BMC Pediatrics

Fig. 1

From: Clinical features of patients with paroxysmal kinesigenic dyskinesia, mutation screening of PRRT2 and the effects of morning draughts of oxcarbazepine

Fig. 1

Chromatograms 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 649

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