GRIN2A-related developmental and/or epileptic encephalopathy with spike-wave activation in sleep

MONDO:1060140

Any developmental and/or epileptic encephalopathy with spike-wave activation in sleep in which the cause of the disease is a variation in GRIN2A gene.

31 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Sort by