nr2f1.org - NR2F1 Foundation - For those with rare NR2F1 gene mutation

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Description: These rare mutations cause a neurodevelopmental disorder called BBSOAS - Bosch-Boonstra-Schaaf optic atrophy syndrome.

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We are a registered 501(c)(3) non-profit organization dedicated to those living with rare variants on the Nr2f1 gene. These variants cause a neurodevelopmental disorder called Bosch-Boonstra-Schaaf optic atrophy syndrome (BBSOAS). { "@context": "https://schema.org", "@type": "Organization", "name": "NR2F1 Foundation", "description": "A nonprofit foundation dedicated to those living with rare mutations on the NR2F1 gene.", "nonprofitStatus" : "Nonprofit501c3", "url": "https://nr2f1.org/", "logo": "https://nr

We are a registered 501(c)(3) non-profit organization dedicated to those living with rare variants on the Nr2f1 gene. These variants cause a neurodevelopmental disorder called Bosch-Boonstra-Schaaf optic atrophy syndrome (BBSOAS). { "@context": "https://schema.org", "@type": "WebPage", "@id": "https://nr2f1.org/#ContentSchema", "headline": "Welcome to the NR2F1 Foundation!", "url": "https://nr2f1.org/", "about": [ {"@type": "Organization", "name": "Charitable_organization", "sameAs": "https://en.wikipedia.o

Our mission at NR2F1 Foundation is to empower families and individuals living with rare NR2F1 variants through education, advocacy and research.

Links to nr2f1.org (3)

• combinedbrain.org Combined Brain
• acrossmatrix.com Matrix
• bbsoas.com NR2F1 Foundation - For those with rare NR2F1 gene mutation