Human genes for Brugada syndrome 4
Brugada syndrome 4 [DOID:0110221]
A Brugada syndrome that has_material_basis_in heterozygous mutation in the gene encoding the beta-2 subunit of the voltage-dependent L-type calcium channel (CACNB2) on chromosome 10p12.
Synonyms: Brugada syndrome 4, DOID:0110221, BRGDA4