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Common and Rare Variants in SCN10A Modulate the Risk of Atrial Fibrillation
BACKGROUND: Genome-wide association studies (GWAS) have shown that the common single nucleotide polymorphism (SNP) rs6800541 located in SCN10A, encoding the voltage-gated Na(v)1.8 sodium channel, is associated with PR–interval prolongation and atrial fibrillation (AF). SNP rs6800541 is in high linka...
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| Veröffentlicht in: | Circ Cardiovasc Genet |
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| Hauptverfasser: | , , , , , , , , , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
2015
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4392342/ https://ncbi.nlm.nih.gov/pubmed/25691686 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/HCG.0000000000000022 |
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