COMMUNITY

GNB1 families are a group of individuals who share a common genetic mutation. This mutation affects the GNB1 gene, which is responsible for producing a protein that helps cells communicate with each other. As a result, those with this mutation may experience a range of symptoms, including developmental delays, seizures, and movement disorders. Despite these challenges, GNB1 families are a resilient and supportive community, coming together to share their experiences and advocate for research and treatment options.