Fig. 2From: Novel variants of SYNGAP1 associated epileptic encephalopathy: two cases report and literature reviewSanger sequencing results of case 1. A denovo heterozygous frameshift mutation in the SYNGAP1 gene: c.3271(exon15)_c.3271(exon15) insT (p.leu1091Leufs*62) (NM_006772) in the proband of case1, and the mutation was not found in the her parentsBack to article page