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
Full text not available from this repository.
| 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 |
| Related URLs: |
|
| Dates: |
| Date | Event |
|---|
| 1 August 2009 | Published |
|
| Web of Science ID: |
WOS:000268432900007 |
  |
Download EPMC Full text (PDF)
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Download EPMC Full text (HTML)
|
| URI: |
https://openaccess.sgul.ac.uk/id/eprint/2051 |
| Publisher's version: |
https://doi.org/10.1038/ng.417 |
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