Supplementary Figure 2: Sanger sequencing chromatograms of one of the case-parent trios with the de novo c.959G>A mutation in KCNC1.
From: A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy
The mutation is indicated by an arrow. Chromatograms for the other Sanger-sequenced trios with the KCNC1 mutation are similar.
