Reactivating the FMR1 Gene to Reverse Fragile X Syndrome

FRAXA Research Foundation is dedicated to funding breakthrough research, providing $240,000 to reactivate the FMR1 gene to combat Fragile X Syndrome, with the goal of restoring vital protein function and advancing towards a cure.

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Unraveling Fragile X Syndrome: New Insights into FMR1 Gene Reactivation

Discover groundbreaking methods for reactivating the FMR1 gene in Fragile X syndrome. Dive into the transformational research and the implications of self-healing at a cellular level.

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FRAXA Funded Research

Current Research Grants (46)