Arid1B Research Foundation
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.
Founded
2022
574
X (Twitter)
103
Address
Chevy Chase
Welcome to FAR | Foundation for ARID1B Research 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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Fund Raising and/or Fund Distribution Category
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