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Chromosome 4q25 variants are genetic modifiers of rare ion channel mutations associated with familial atrial fibrillation
OBJECTIVES: This study tested the hypothesis that two common polymorphisms in the chromosome 4q25 region that have been associated with atrial fibrillation (AF) contribute to the variable penetrance of familial AF. BACKGROUND: Although mutations in ion channels, gap junction proteins, and signaling...
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| 主要な著者: | , , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2012
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3448817/ https://ncbi.nlm.nih.gov/pubmed/22818067 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jacc.2012.04.030 |
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