Fragile X Syndrome Using Patient-derived Stem Cell Versions Delicate X Syndrome (FXS) is normally due to an expansion of CGG trinucleotide repeats in the 5′ untranslated region from the (promoter that leads to epigenetic silencing SYN-115 from the gene and FMRP protein deficiency. created individual FXS stem cell versions. Evaluation of FXS-affected individual embryonic stem… Continue reading Fragile X Syndrome Using Patient-derived Stem Cell Versions Delicate X Syndrome