Fig. 2From: Identification of deep intronic variants of PAH in phenylketonuria using full-length gene sequencingIn Silico prediction of deep intronic variants. A ESEfinder predicted that the c.706+531T>C might create an SRSF1 (SF2/ASF(IgM-BRCA1)) binding sites; B ESEfinder predicted that the c.706+608A>C variant may strengthen the SRSF2 (SC35) binding sitesBack to article page