Crowdstake

NR2F1 Foundation

EIN: 83-2659721 · Royal Oak, MI

Research on BBSOAS
Advocacy for Affected Families
Education about the Condition

Our Story

The NR2F1 Foundation is dedicated to supporting individuals and families impacted by Bosch-Boonstra-Schaaf optic atrophy syndrome (BBSOAS), a rare neurodevelopmental disorder caused by variants in the Nr2f1 gene. Through education, advocacy, and research, the foundation strives to empower those affected by this condition.

Impact

With over $130,000 raised, the NR2F1 Foundation is funding vital research projects aimed at discovering biomarkers for BBSOAS and developing new mouse models for further study.

Make a Difference Today

Join the fight against BBSOAS by donating cryptocurrency or cash to the NR2F1 Foundation. Your contribution can help change lives and bring hope to families affected by this rare condition.

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