GRIN2A-related self-limited epilepsy with centrotemporal spikes

MONDO:1060142

Any self-limited epilepsy with centrotemporal spikes in which the cause of the disease is a variation in GRIN2A gene.

11 clinical trials for this condition and its sub-types, 0 tagged with GRIN2A-related self-limited epilepsy with centrotemporal spikes itself.

Where it sits in the disease tree

Part of

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.