GRIN2A-related rolandic epilepsy-speech dyspraxia syndrome

MONDO:1060141

Any rolandic epilepsy-speech dyspraxia syndrome in which the cause of the disease is a variation in GRIN2A gene.

9 clinical trials for this condition and its sub-types, 0 tagged with GRIN2A-related rolandic epilepsy-speech dyspraxia syndrome itself.

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