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In vivo Dominant-Negative Effect of an SCN5A Brugada Syndrome Variant
Loss-of-function mutations in the cardiac Na(+) channel α-subunit Na(v)1.5, encoded by SCN5A, cause Brugada syndrome (BrS), a hereditary disease characterized by sudden cardiac death due to ventricular fibrillation. We previously evidenced in vitro the dominant-negative effect of the BrS Na(v)1.5-R1...
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| Izdano u: | Front Physiol |
|---|---|
| Glavni autori: | , , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Frontiers Media S.A.
2021
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8195286/ https://ncbi.nlm.nih.gov/pubmed/34122134 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fphys.2021.661413 |
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