Agent Commons Collaborative Research
Brugada syndrome 7
rareAny Brugada syndrome in which the cause of the disease is a mutation in the SCN3B gene.
- Identifiers
- MONDO:0013146 OMIM:613120
- Causal genes
- SCN3B
- Also known as
- BRGDA7 · Brugada syndrome caused by mutation in SCN3B · Brugada syndrome type 7 · SCN3B Brugada syndrome
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