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Endemic polycythemia in Russia: mutation in the VHL gene.
Ang SO, Chen H, Gordeuk VR, Sergueeva AI, Polyakova LA, Miasnikova GY, Kralovics R, Stockton DW, Prchal JT. Ang SO, et al. Among authors: stockton dw. Blood Cells Mol Dis. 2002 Jan-Feb;28(1):57-62. doi: 10.1006/bcmd.2002.0488. Blood Cells Mol Dis. 2002. PMID: 11987242
Disruption of oxygen homeostasis underlies congenital Chuvash polycythemia.
Ang SO, Chen H, Hirota K, Gordeuk VR, Jelinek J, Guan Y, Liu E, Sergueeva AI, Miasnikova GY, Mole D, Maxwell PH, Stockton DW, Semenza GL, Prchal JT. Ang SO, et al. Among authors: stockton dw. Nat Genet. 2002 Dec;32(4):614-21. doi: 10.1038/ng1019. Epub 2002 Nov 4. Nat Genet. 2002. PMID: 12415268
The worldwide distribution of the VHL 598C>T mutation indicates a single founding event.
Liu E, Percy MJ, Amos CI, Guan Y, Shete S, Stockton DW, McMullin MF, Polyakova LA, Ang SO, Pastore YD, Jedlickova K, Lappin TR, Gordeuk V, Prchal JT. Liu E, et al. Among authors: stockton dw. Blood. 2004 Mar 1;103(5):1937-40. doi: 10.1182/blood-2003-07-2550. Epub 2003 Nov 6. Blood. 2004. PMID: 14604959 Free article.
Congenital polycythemias/erythrocytoses.
Gordeuk VR, Stockton DW, Prchal JT. Gordeuk VR, et al. Among authors: stockton dw. Haematologica. 2005 Jan;90(1):109-16. Haematologica. 2005. PMID: 15642677 Review.
71 results