Brugada syndrome 5 (Q27677687)
Jump to navigation
Jump to search
Brugada syndrome that has material basis in heterozygous mutation in the SCN1B gene on chromosome 19q13
- BRGDA5
- Brugada syndrome type 5
- BRUGADA SYNDROME 5; BRGDA5
- Cardiac Conduction Defect, Nonspecific
- BRUGADA SYNDROME 5
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Brugada syndrome 5 |
Brugada syndrome that has material basis in heterozygous mutation in the SCN1B gene on chromosome 19q13 |
|
Statements
1 reference
1 reference
Identifiers
1 reference
2 references
1 reference
1 reference
1 reference
1 reference