Arid1B Research Foundation

Welcome to FAR | Foundation for ARID1B Research

Accelerating the development of disease-modifying treatments for #ARID1B-RD (haploinsufficiency) - the most frequently mutated gene in de novo NDDs (ASD, ID). FAR is a parent-led organization kick-starting research to find life-changing treatments for ARID1B-related disorder. To advance the scientific and clinical understanding of disorders associated with ARID1B gene and the development of potential therapies for such disorders.
881940774
EIN
2022
Founded
Chevy Chase, MD 20825 United States
Address
arid1b.org
Web
FAR_ARID1B
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We go FARther in developing lifechanging treatments for ARID1BRD. Support our macthed campaign. We are a group of parents fighting for a better future for our children and generations to come. Huge strides are being made in treatments for rare genetic conditions.

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