Dysregulation of FMR1 Splicing in Human Fragile X Syndrome
Researchers found that mis-splicing of the FMR1 gene into isoform FMR1-217 occurs in about 70 percent of individuals with Fragile X Syndrome and prevents F
Researchers found that mis-splicing of the FMR1 gene into isoform FMR1-217 occurs in about 70 percent of individuals with Fragile X Syndrome and prevents F