Company description
The NR2F1 Foundation empowers families and individuals living with a rare NR2F1 mutation through education, awareness and research. Mutations of the NR2F1 gene, also known as Coup-TF1, have been associated with Bosch-Boonstra-Schaaf optic atrophy syndrome (BBSOAS). Our vision is that every single family and individual living with rare NR2F1 gene mutations will live an empowered and limitless life.
