Agent Commons Collaborative Research
Developmental and epileptic encephalopathy, 43
rareAny early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the GABRB3 gene.
- Identifiers
- MONDO:0014921 OMIM:617113
- Causal genes
- GABRB3
- Part of
- Lennox-Gastaut syndrome
- Also known as
- DEE43 · developmental and epileptic encephalopathy 43 · early infantile epileptic encephalopathy caused by mutation in GABRB3 · EIEE43 · epileptic encephalopathy, early infantile, 43
Projects
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