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A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke

Gudbjartsson, DF; Holm, H; Gretarsdottir, S; Thorleifsson, G; Walters, GB; Thorgeirsson, G; Gulcher, J; Mathiesen, EB; Njølstad, I; Nyrnes, A; et al. Gudbjartsson, DF; Holm, H; Gretarsdottir, S; Thorleifsson, G; Walters, GB; Thorgeirsson, G; Gulcher, J; Mathiesen, EB; Njølstad, I; Nyrnes, A; Wilsgaard, T; Hald, EM; Hveem, K; Stoltenberg, C; Kucera, G; Stubblefield, T; Carter, S; Roden, D; Ng, MC; Baum, L; So, WY; Wong, KS; Chan, JC; Gieger, C; Wichmann, HE; Gschwendtner, A; Dichgans, M; Kuhlenbäumer, G; Berger, K; Ringelstein, EB; Bevan, S; Markus, HS; Kostulas, K; Hillert, J; Sveinbjörnsdóttir, S; Valdimarsson, EM; Løchen, ML; Ma, RC; Darbar, D; Kong, A; Arnar, DO; Thorsteinsdottir, U; Stefansson, K (2009) A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke. NATURE GENETICS, 41 (8). 876 - 878 (3). ISSN 1061-4036 https://doi.org/10.1038/ng.417
SGUL Authors: Bevan, Stephen Nicholas Markus, Hugh Stephen

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Item Type: Article
Additional Information: PubMed ID: 19597491
Keywords: Science & Technology, Life Sciences & Biomedicine, Genetics & Heredity, CHROMOSOME 4Q25, ATBF1, RISK, METAANALYSIS, PROTEIN, Atrial Fibrillation, Base Sequence, Brain Ischemia, Chromosomes, Human, Pair 16, Genetic Predisposition to Disease, Homeodomain Proteins, Humans, Mutation, Stroke
Journal or Publication Title: NATURE GENETICS
ISSN: 1061-4036
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Dates:
DateEvent
1 August 2009Published
Web of Science ID: WOS:000268432900007
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URI: http://openaccess.sgul.ac.uk/id/eprint/2051
Publisher's version: https://doi.org/10.1038/ng.417

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