(Q27677685)

English

Brugada syndrome 4

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

  • BRGDA4
  • BRUGADA SYNDROME 4
  • BRUGADA SYNDROME 4; BRGDA4
  • Brugada syndrome type 4

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Identifiers

 
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