Roughly 100 people are known to be impacted by a GNAO1 related neurodevelopmental disorder.
Most patients have been diagnosed in the past year or two.
What We Do
The Bow Foundation supports GNAO1 families by raising awareness, enhancing research, and fostering community.
To date about 100 people worldwide have been identified as having a mutation on the GNAO1 gene.
We fund cutting edge research into GNAO1–related neurodevelopmental disorders and similar rare diseases.
Read stories from some of the roughly 100 people impacted by a GNAO1 disorder.
Your donation will help fund GNAO1 medical research and change lives. No amount is too small.