FamilieSCN2A Foundation
FamilieSCN2A is an organization created by parents of children diagnosed with rare forms of Epilepsy and Autism as a result of a change in the SCN2A gene.
SCN2A is the name of a gene that is commonly associated with early-onset epilepsy and is a leading genetic cause of autism spectrum disorder.
The FamilieSCN2A Foundation’s mission is to accelerate research, build community, and advocate to improve the lives of ALL those affected by SRDs around the world.
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