Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits-Reference-Cited by-同舟云学术

Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits

Published:2014-04-28 Issue:6 Volume:46 Page:629-634
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Auer Paul L,Teumer Alexander^ORCID,Schick Ursula,O'Shaughnessy Andrew,Lo Ken Sin,Chami Nathalie,Carlson Chris,de Denus Simon,Dubé Marie-Pierre,Haessler Jeff,Jackson Rebecca D,Kooperberg Charles,Perreault Louis-Philippe Lemieux,Nauck Matthias,Peters Ulrike,Rioux John D,Schmidt Frank,Turcot Valérie,Völker Uwe,Völzke Henry,Greinacher Andreas,Hsu Li,Tardif Jean-Claude,Diaz George A,Reiner Alexander P,Lettre Guillaume

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.2962.pdf

Reference51 articles.

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3. van der Harst, P. et al. Seventy-five genetic loci influencing the human red blood cell. Nature 492, 369–375 (2012).

4. Zhou, Z. et al. USF and NF-E2 cooperate to regulate the recruitment and activity of RNA polymerase II in the β-globin gene locus. J. Biol. Chem. 285, 15894–15905 (2010).

5. de la Chapelle, A., Sistonen, P., Lehvaslaiho, H., Ikkala, E. & Juvonen, E. Familial erythrocytosis genetically linked to erythropoietin receptor gene. Lancet 341, 82–84 (1993).

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