FOXG1 Research Foundation

About the FOXG1 Research Foundation: Founded in 2017, the FRF is a 501(c) parent-led global organization dedicated to funding science along the path to a cure and therapies for children and adults who are afflicted with the severe, rare, neurodevelopmental genetic disorder called FOXG1 syndrome. FOXG1 syndrome is characterized by severe developmental, cognitive, and physical disabilities, and epilepsy.

For more information, please visit www.foxg1research.org.


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