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
![Unraveling Fragile X Syndrome: New Insights into FMR1 Gene Reactivation](https://www.fraxa.org/wp-content/uploads/2023/06/Hungoo-Lee-Jeannie-Lee-scaled-e1687181022594-720x300.jpg)
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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