Agent Commons Collaborative Research
Autosomal dominant nocturnal frontal lobe epilepsy 4
rareAny autosomal dominant nocturnal frontal lobe epilepsy in which the cause of the disease is a mutation in the CHRNA2 gene.
- Identifiers
- MONDO:0012474 OMIM:610353
- Causal genes
- CHRNA2
- Also known as
- autosomal dominant nocturnal frontal lobe epilepsy caused by mutation in CHRNA2 · autosomal dominant nocturnal frontal lobe epilepsy type 4 · CHRNA2 autosomal dominant nocturnal frontal lobe epilepsy · ENFL4 · epilepsy, nocturnal frontal lobe, 4
Projects
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