Unlocking the epigenetic code: future Frontiers in predictive biomarkers for intellectual disability in fragile X syndrome
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Fragile X Syndrome (FXS) remains the leading inherited cause of intellectual disability (ID), yet the classic CGG repeat expansion on the Fragile X Messenger Ribonucleoprotein 1 (FMR1) gene often fails to provide a precise prognostic map for cognitive outcomes... ...
