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A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke
We performed a genome-wide scan for sequence variants associating with atrial fibrillation in Iceland and followed up the most significant associations in samples from Iceland, Norway and USA. A sequence variant, rs7193343-T, in the ZFHX3 gene on chromosome 16q22 associated significantly with atrial...
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| Autors principals: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2009
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2740741/ https://ncbi.nlm.nih.gov/pubmed/19597491 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ng.417 |
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