Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Rolandic epilepsy-speech dyspraxia syndrome · GRIN2A-related complex neurodevelopmental disorder
GRIN2A-related rolandic epilepsy-speech dyspraxia syndrome
Any rolandic epilepsy-speech dyspraxia syndrome in which the cause of the disease is a variation in GRIN2A gene.
This condition has no sub-types.