In silico validation revealed the role of SCN5A mutations and their genotype–phenotype correlations in Brugada syndrome
Abstract Background Brugada syndrome (BrS) is a rare genetic disease that causes sudden cardiac death (SCD) and arrhythmia. SCN5A pathogenic variants (about 30% of diagnosed patients) are responsible for BrS. Aims Lack of knowledge regarding molecular characteristics and the correlation between geno...
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| Principais autores: | , , , , , , , , , , , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Wiley
2023-12-01
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| Serier: | Molecular Genetics & Genomic Medicine |
| Fag: | |
| Online adgang: | https://doi.org/10.1002/mgg3.2263 |
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