Human genes for Brugada syndrome 3
Brugada syndrome 3 [DOID:0110220]
A 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.
Synonyms: Brugada syndrome 3, DOID:0110220, BRGDA3