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, 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
Nat Genet. 2009 41 (8): 876-8

PMID: 19597491 · PMCID: PMC2740741 · DOI:10.1038/ng.417

MeSH Terms (9)

Atrial Fibrillation Base Sequence Brain Ischemia Chromosomes, Human, Pair 16 Genetic Predisposition to Disease Homeodomain Proteins Humans Mutation Stroke

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