# Brugada syndrome 3

> Brugada syndrome that has material basis in heterozygous mutation in the gene encoding the alpha-1C subunit of the L-type voltage-dependent calcium channel (CACNA1C) on chromosome 12p13

**Wikidata**: [Q27677684](https://www.wikidata.org/wiki/Q27677684)  
**Source**: https://4ort.xyz/entity/brugada-syndrome-3


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Brugada syndrome: report of the second consensus conference: endorsed by the Heart Rhythm Society and the European Heart Rhythm Association.
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)