GRIN2B Foundation

GRIN2B is a gene located on the short arm (called “p”) of the 12th chromosome at 12p13.1. This neurological condition is often characterized by low muscle tone, developmental delays, seizures and lack of speech. The spectrum of abilities is quite broad depending on the exact genetic variation. Some of our children cannot walk or talk, and most struggle to communicate their most basic daily needs.GRIN2B Foundation is a parent-run organization dedicated to furthering research on the GRIN2B gene and providing support and education to the small, but growing community of individuals and families impacted by a GRIN2B diagnosis.