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. 2022 Jun 22;10:919996. doi: 10.3389/fped.2022.919996

Figure 4.

Figure 4

(A) Chromatogram of Sanger sequencing showing one base pair insertion of “G” nucleotide in exon 3 of CACNB4 gene sequence of c.78_79insG, p.Asp27Glyfs*26 in three different patients from the cohort of 25 epileptic sporadic patients leading to a frameshift mutation. (B) Chromatogram of Sanger sequencing showing wild-type sequence of the CACNB4 gene (obtained from 100 healthy individuals as the control group).