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

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Title:	A rare splice donor mutation in the haptoglobin gene associates with blood lipid levels and coronary artery disease.
Author(s):	Bjornsson, E.; Halldorsson, G.; Helgadottir, A.; Gylfason, A; Kehr, B.; Jonasdottir, A.; Sigurdsson, A.; Oddsson, A.; Thorleifsson, G.; Magnusson, O.T.; Gretarsdottir, S.; 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.
Publication year:	2017
Source:	Human Molecular Genetics, vol. 26, iss. 12, (2017), pp. 2364-2376
ISSN:	0964-6906
DOI:	https://doi.org/10.1093/hmg/ddx123
Publication type:	Article / Letter to editor
Please use this identifier to cite or link to this item : https://hdl.handle.net/2066/174137
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Subject:	Radboudumc 11: Renal disorders RIMLS: Radboud Institute for Molecular Life Sciences Radboudumc 15: Urological cancers RIHS: Radboud Institute for Health Sciences
Organization:	Laboratory Medicine Health Evidence Urology
Journal title:	Human Molecular Genetics
Volume:	vol. 26
Issue:	iss. 12
Page start:	p. 2364
Page end:	p. 2376

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