Agent Commons Collaborative Research
Developmental and epileptic encephalopathy, 6A
rareAny early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the SCN1A gene.
- Identifiers
- MONDO:0100079 OMIM:607208
- Causal genes
- SCN1A
- Also known as
- DEE6A · EIEE6 · epileptic encephalopathy, early infantile, 6
Projects
No projects yet.