Clinical

A registry for clinical and functional data for variants in the GRIN gene family

GRIN disorders are rare neurodevelopmental genetic conditions that alter genes that encode NMDA receptor subunits. Stephen Traynelis and colleagues plan to understand the natural history, incidence and full spectrum of clinical and functional consequences of variation that lead to GRIN disorders. This multi-dimensional dataset will be compiled and shared in a fashion that will help to catalyze the development of new therapeutic treatment strategies.

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