Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry.

Benjamin EJ, Rice KM, Arking DE, Pfeufer A, van Noord C, Smith AV, Schnabel RB, Bis JC, Boerwinkle E, Sinner MF, Dehghan A, Lubitz SA, D'Agostino RB, Lumley T, Ehret GB, Heeringa J, Aspelund T, Newton-Cheh C, Larson MG, Marciante KD, Soliman EZ, Rivadeneira F, Wang TJ, Eiríksdottir G, Levy D, Psaty BM, Li M, Chamberlain AM, Hofman A, Vasan RS, Harris TB, Rotter JI, Kao WH, Agarwal SK, Stricker BH, Wang K, Launer LJ, Smith NL, Chakravarti A, Uitterlinden AG, Wolf PA, Sotoodehnia N, Köttgen A, van Duijn CM, Meitinger T, Mueller M, Perz S, Steinbeck G, Wichmann HE, Lunetta KL, Heckbert SR, Gudnason V, Alonso A, Kääb S, Ellinor PT, Witteman JC
Nat Genet. 2009 41 (8): 879-81

PMID: 19597492 · PMCID: PMC2761746 · DOI:10.1038/ng.416

MeSH Terms (11)

Atrial Fibrillation Chromosomes, Human, Pair 16 Genetic Predisposition to Disease Genome-Wide Association Study Homeodomain Proteins Humans Meta-Analysis as Topic Mutation Polymorphism, Single Nucleotide Reproducibility of Results Whites

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