Brugada syndrome 3 (Q27677684)

From Wikidata
Jump to navigation Jump to search
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
  • BRGDA3
  • Brugada syndrome type 3
  • BRUGADA SYNDROME 3
  • BRUGADA SYNDROME 3; BRGDA3
edit
Language Label Description Also known as
English
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
  • BRGDA3
  • Brugada syndrome type 3
  • BRUGADA SYNDROME 3
  • BRUGADA SYNDROME 3; BRGDA3

Statements

Identifiers

 
edit
    edit
      edit
        edit
          edit
            edit
              edit
                edit
                  edit