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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Manylion Llyfryddiaeth
Prif Awduron: Gudbjartsson, Daniel F., Holm, Hilma, Gretarsdottir, Solveig, Thorleifsson, Gudmar, Walters, G. Bragi, Thorgeirsson, Gudmundur, Gulcher, Jeffrey, Mathiesen, Ellisiv, Njølstad, Inger, Nyrnes, Audhild, Wilsgaard, Tom, Hald, Erin, Hveem, Kristian, Stoltenberg, Camilla, Kucera, Gayle, Stubblefield, Tanya, Carter, Shannon, Roden, Dan, Ng, Maggie C.Y., Baum, Larry, So, Wing Yee, Wong, Ka Sing, Chan, Juliana C. N., Gieger, Christian, Wichmann, H-Erich, Gschwendtner, Andreas, Dichgans, Martin, Kuhlenbäumer, Gregor, Berger, Klaus, Ringelstein, E. Bernd, Bevan, Steve, Markus, Hugh, Kostulas, Konstantinos, Hillert, Jan, Sveinbjörnsdóttir, Sigurlaug, Valdimarsson, Einar M., Løchen, Maja-Lisa, Ma, Ronald C. W., Darbar, Dawood, Kong, Augustine, Arnar, David O., Thorsteinsdottir, Unnur, Stefansson, Kari
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 2009
Pynciau:
Article
Mynediad Ar-lein: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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