(Q27677684)
Statements
1 reference
1 reference
Identifiers
1 reference
1 reference
2 references
2 references
1 reference
1 reference
1 reference
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