A rare splice donor mutation in the haptoglobin gene associates with blood lipid levels and coronary artery disease.

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Publication year
2017
Author(s)
Bjornsson, E.
Helgason, H.
Halldorsson, G.
Helgadottir, A.
Gylfason, A
Kehr, B.
Jonasdottir, A.
Sigurdsson, A.
Oddsson, A.
Thorleifsson, G.
Magnusson, O.T.
Gretarsdottir, S.
Zink, F.
Kristjansson, R.P.
Asgeirsdottir, M.
Swinkels, D.W.
Kiemeney, L.A.
Eyjolfsson, G.I.
Sigurdardottir, O.
Masson, G.
Olafsson, I.
Thorgeirsson, G.
Holm, H.
Thorsteinsdottir, U.
Gudbjartsson, D.F.
Sulem, P.
Stefansson, K.
Source
Human Molecular Genetics, 26, 12, (2017), pp. 2364-2376
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DOI
Publication type
Article / Letter to editor
Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/174137   https://hdl.handle.net/2066/174137
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