Fig. 7From: PRRT2 gene variant in a child with dysmorphic features, congenital microcephaly, and severe epileptic seizures: genotype-phenotype correlation?Analysis in silico of putative TFs using PROMO predicted for the coding consensus sequencing of PRRT2 gene. Output modified from PROMO result showing the binding sites of TFs overlapping the variant c.501 C > T in the exon 2 of the PRRT2 geneBack to article page