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. 2017 Apr 7;7:46227. doi: 10.1038/srep46227

Figure 2. Percentage of Cases with Variants Among All the Variants Identified in Our Study.

Figure 2

Among the 13 cases with detected variants, SCN1A was the most frequently affected gene in our study, accounting for 38.5%, followed by STXBP1, CDKL5, KCNQ2, ARX and SCN8A of 15.4%, 15.4%, 15.4%, 7.7% and 7.7% respectively.