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

Gudbjartsson, DF (author)

Holm, H (author)

Gretarsdottir, S (author)

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Thorleifsson, G (author)

Walters, GB (author)

Thorgeirsson, G (author)

Gulcher, J (author)

Mathiesen, EB (author)

Njolstad, I (author)

Nyrnes, A (author)

Wilsgaard, T (author)

Hald, EM (author)

Hveem, K (author)

Stoltenberg, C (author)

Kucera, G (author)

Stubblefield, T (author)

Carter, S (author)

Roden, D (author)

Ng, MCY (author)

Baum, L (author)

So, WY (author)

Wong, KS (author)

Chan, JCN (author)

Gieger, C (author)

Wichmann, HE (author)

Gschwendtner, A (author)

Dichgans, M (author)

Kuhlenbaumer, G (author)

Berger, K (author)

Ringelstein, EB (author)

Bevan, S (author)

Markus, HS (author)

Kostulas, K (author)

Karolinska Institutet

Hillert, J (author)

Karolinska Institutet

Sveinbjornsdottir, S (author)

Valdimarsson, EM (author)

Lochen, ML (author)

Ma, RCW (author)

Darbar, D (author)

Kong, A (author)

Arnar, DO (author)

Thorsteinsdottir, U (author)

Stefansson, K (author)

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 (creator_code:org_t)

2009-07-13

2009

English.

In: Nature genetics. - : Springer Science and Business Media LLC. - 1546-1718 .- 1061-4036. ; 41:8, s. 876-878

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• Journal article (peer-reviewed)