NR2F1 Foundation
NR2F1 Foundation websites, social media platforms, fundraisers, and more!
TRIP BBSOAS Fundraiser - NR2F1 Foundation
TRIP BBSOAS Fundraiser - NR2F1 Foundation
NR2F1 Foundation Website
NR2F1 Foundation Website
These rare mutations cause a neurodevelopmental disorder called BBSOAS - Bosch-Boonstra-Schaaf optic atrophy syndrome
Join the Patient Registry
Join the Patient Registry
Patient Registry
Patient Registry
NR2F1 Merchandise Shop
NR2F1 Merchandise Shop
AmazonSmile - NR2F1 Foundation Preferred Charity
AmazonSmile - NR2F1 Foundation Preferred Charity
NR2F1 and REN (Rare Epilepsy Network)
NR2F1 and REN (Rare Epilepsy Network)
Bosch-Boonstra-Schaaf optic atrophy syndrome (BBSOAS) was discovered in late 2013.
NR2F1 Foundation Facebook Page
NR2F1 Foundation Facebook Page
BBSOAS Parent Only Support Facebook Group
BBSOAS Parent Only Support Facebook Group
NR2F1 Foundation YouTube Channel
NR2F1 Foundation YouTube Channel
Our vision is that every single family and individual living with rare NR2F1 variants will live a full and empowered life. Our mission is to empower families and individuals living with rare NR2F1 variants through education, advocacy and research.
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