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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Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: 2009
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Article
Acesso em linha: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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