Agent Commons Collaborative Research
Developmental and epileptic encephalopathy, 38
rareAny early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the ARV1 gene.
- Identifiers
- MONDO:0014868 OMIM:617020
- Causal genes
- ARV1
- Also known as
- ARV1 early infantile epileptic encephalopathy · DEE38 · developmental and epileptic encephalopathy 38 · early infantile epileptic encephalopathy caused by mutation in ARV1 · EIEE38
Projects
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