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A rare splice donor mutation in the haptoglobin gene associ..:
Bjornsson, Eythor
;
Helgason, Hannes
;
Halldorsson, Gisli
...
Human Molecular Genetics. 26 (2017) 12 - p. 2364-2376 , 2017
Link:
https://doi.org/10.1093/hmg/ddx123
RT Journal T1
A rare splice donor mutation in the haptoglobin gene associates with blood lipid levels and coronary artery disease
UL https://suche.suub.uni-bremen.de/peid=cr-10.1093_hmg_ddx123&Exemplar=1&LAN=DE A1 Bjornsson, Eythor A1 Helgason, Hannes A1 Halldorsson, Gisli A1 Helgadottir, Anna A1 Gylfason, Arnaldur A1 Kehr, Birte A1 Jonasdottir, Adalbjorg A1 Jonasdottir, Aslaug A1 Sigurdsson, Asgeir A1 Oddsson, Asmundur A1 Thorleifsson, Gudmar A1 Magnusson, Olafur Th. A1 Gretarsdottir, Solveig A1 Zink, Florian A1 Kristjansson, Ragnar P. A1 Asgeirsdottir, Margret A1 Swinkels, Dorine W. A1 Kiemeney, Lambertus A. A1 Eyjolfsson, Gudmundur I. A1 Sigurdardottir, Olof A1 Masson, Gisli A1 Olafsson, Isleifur A1 Thorgeirsson, Gudmundur A1 Holm, Hilma A1 Thorsteinsdottir, Unnur A1 Gudbjartsson, Daniel F. A1 Sulem, Patrick A1 Stefansson, Kari PB Oxford University Press (OUP) YR 2017 SN 0964-6906 SN 1460-2083 JF Human Molecular Genetics VO 26 IS 12 SP 2364 OP 2376 LK http://dx.doi.org/https://doi.org/10.1093/hmg/ddx123 DO https://doi.org/10.1093/hmg/ddx123 SF ELIB - SuUB Bremen
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