Every two months, we’ll be sharing updates on the latest publications about GRIN genes, NMDA receptors and other glutamate receptors.

CureGRIN’s end of year report.

Every two months, we’ll be sharing updates on the latest publications about GRIN genes, NMDA receptors and other glutamate receptors.

CureGRIN Foundation is pleased to announce an investment of $75,000 to cover the cost of functional analysis for 50 people with GRIN Disorder. The recipient of CureGRIN’s grant the Center for Functional Evaluation of Rare Variants (CFERV), led by Stephen Traynelis, PhD and Director. CFERV’s mission is to advance the scientific understanding of rare genetic variants that cause ultra-rare genetic conditions such as GRIN Disorder.

Every two months, we’ll be sharing updates on the latest publications about GRIN genes, NMDA receptors and other glutamate receptors.

We recently asked family members of the GRIN Disorder community about their concerns and challenges with the medical system.

When we become parents of rare disease kids, we’re expected to become everything from physiotherapist to pharmacist overnight. This post is a primer to help you embrace your inner geneticist.

This eight-part series tells the story of Bryson, GRIN Disorder, and Keith’s family’s search for a cure.

Big news! We are thrilled to share that Austin’s Purpose, the first charity to raise funds for GRIN Disorders, will join forces with us and become part of CureGRIN. Austin’s