CureGRIN is a parent-led foundation committed to improving the lives of people living with GRIN Disorders.
Our goal is simple and bold: To find cures and therapies for people living with disorders caused by variants in the GRIN1, GRIN2A, GRIN2B, and GRIN2D genes.
GRIN Disorders are caused by a change in one of the seven GRIN genes. These genes contain the code to create NMDA receptors, which are essential for learning and memory.
© 2020 by CureGRIN Foundation
The CureGRIN Foundation is a registered 501(c)(3) foundation.