Brugada syndrome 3 (Q27677684)
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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
Language | Label | Description | Also known as |
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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 |
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