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Developmental and epileptic encephalopathy, 6A

MONDO:0100079

Any early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the SCN1A gene.

Also known as: DEE6A, EIEE6, developmental and epileptic encephalopathy, 6A, epileptic encephalopathy, early infantile, 6, Dravet syndrome

17 clinical trials for this condition and its sub-types, 0 tagged with Developmental and epileptic encephalopathy, 6A itself.

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