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Percy MJ, Sanchez M, Swierczek S, et al. 
Is congenital secondary erythrocytosis/polycythemia caused by activating mutations within the HIF-2 alpha iron-responsive element? [Letter]
Blood 2007 Oct 1; 110(7):2776-7.
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Percy MJ, Beer PA, Campbell G, et al. 
Novel Exon 12 mutations in the HIF2A gene associated with erythrocytosis. [JOURNAL ARTICLE]
Blood 2008 Mar 31.
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Percy MJ 
Familial erythrocytosis arising from a gain-of-function mutation in the HIF2A gene of the oxygen sensing pathway. [Journal Article]
Ulster Med J 2008 May; 77(2):86-8.
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Percy MJ, Furlow PW, Lucas GS, et al. 
A gain-of-function mutation in the HIF2A gene in familial erythrocytosis. [Case Reports, Journal Article, Research Support, N.I.H., Extramural]
N Engl J Med 2008 Jan 10; 358(2):162-8.
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Gale DP, Harten SK, Reid CD, et al. 
Autosomal dominant erythrocytosis and pulmonary arterial hypertension associated with an activating HIF2 alpha mutation. [Letter, Research Support, Non-U.S. Gov't]
Blood 2008 Aug 1; 112(3):919-21.
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Pastore Y, Jedlickova K, Guan Y, et al. 
Mutations of von Hippel-Lindau tumor-suppressor gene and congenital polycythemia. [Case Reports, Journal Article]
Am J Hum Genet 2003 Aug; 73(2):412-9.
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Eltzschig HK, El Kasmi KC, Eckle T 
The HIF2A gene in familial erythrocytosis. [Comment, Letter]
N Engl J Med 2008 May 1; 358(18):1965-6; author reply 1966-7.
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Perrotta S, Della Ragione F 
The HIF2A gene in familial erythrocytosis. [Comment, Letter]
N Engl J Med 2008 May 1; 358(18):1966; author reply 1966-7.
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Percy MJ, Furlow PW, Beer PA, et al. 
A novel erythrocytosis-associated PHD2 mutation suggests the location of a HIF binding groove. [JOURNAL ARTICLE]
Blood 2007 Jun 19.
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