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675 related items for PubMed ID: 15727249

  • 1. Frequency of HFE H63D, S65C, and C282Y mutations in patients with iron overload and controls from Toledo, Spain.
    de Diego C, Murga MJ, Martínez-Castro P.
    Genet Test; 2004; 8(3):263-7. PubMed ID: 15727249
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  • 3. HFE gene C282Y, H63D and S65C mutations frequency in the Transylvania region, Romania.
    Trifa AP, Popp RA, Militaru MS, Farcaş MF, Crişan TO, Gana I, Cucuianu A, Pop IV.
    J Gastrointestin Liver Dis; 2012 Jun; 21(2):177-80. PubMed ID: 22720307
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  • 4. Low frequency of HFE gene mutations in Croatian patients suspected of having hereditary hemochromatosis.
    Milić S, Ristić S, Starčević-Čizmarević N, Brajenović-Milić B, Crnić-Martinović M, Kapović M, Peterlin B, Štimac D.
    Med Sci Monit; 2011 Oct; 17(10):CR552-6. PubMed ID: 21959608
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  • 5. Frequency of the hemochromatosis HFE mutations C282Y, H63D, and S65C in blood donors in the Faroe Islands.
    Milman N, á Steig T, Koefoed P, Pedersen P, Fenger K, Nielsen FC.
    Ann Hematol; 2005 Mar; 84(3):146-9. PubMed ID: 15042317
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  • 6. Analysis of the HFE gene (C282Y, H63D and S65C) mutations in a general Chinese Han population.
    Lin A, Yan WH, Xu HH, Zhu M, Zhou MY.
    Tissue Antigens; 2007 Sep; 70(3):252-5. PubMed ID: 17661915
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  • 7. Prevalence of the C282Y, H63D, and S65C mutations of the HFE gene in 1,146 newborns from a region of Northern Spain.
    Altes A, Ruiz A, Barceló MJ, Remacha AF, Puig T, Maya AJ, Castell C, Amate JM, Saz Z, Baiget M.
    Genet Test; 2004 Sep; 8(4):407-10. PubMed ID: 15684872
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  • 8. S65C and other mutations in the haemochromatosis gene in the Czech population.
    Cimburová M, Půtová I, Provazníková H, Pintérová D, Horák J.
    Folia Biol (Praha); 2005 Sep; 51(6):172-6. PubMed ID: 16419611
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  • 12. Analysis of HFE genes C282Y, H63D, and S65D in patients with hyperferritinemia from northeastern Brazil.
    Leão GD, Freire JM, Cunha Fernandes AL, Moura de Oliveira TM, Leão ND, Gil EA, de Vasconcelos RC, Azevedo JP, de Farias Sales VS, de Araújo Moura Lemos TM, Leão MD, do Nascimento FF, Maciel JF, de Freitas RV, de Souza Paiva A, Cavalcanti GB.
    J Clin Lab Anal; 2014 May; 28(3):178-85. PubMed ID: 24395214
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  • 13. Mutation analysis of the HFE gene associated with hereditary hemochromatosis in a Venezuelan sample.
    Vizzi E, Loureiro CL, Gerder M, de las Nieves Garcia-Casal M, Rodríguez-Larralde A, Gerace L, Ludert JE, Liprandi F, Pujol FH.
    Ann Hematol; 2005 Nov; 84(12):802-6. PubMed ID: 15995871
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  • 14. Two novel missense mutations of the HFE gene (I105T and G93R) and identification of the S65C mutation in Alabama hemochromatosis probands.
    Barton JC, Sawada-Hirai R, Rothenberg BE, Acton RT.
    Blood Cells Mol Dis; 1999 Nov; 25(3-4):147-55. PubMed ID: 10575540
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  • 15. Hereditary hemochromatosis: the clinical significance of the S65C mutation.
    Asberg A, Thorstensen K, Hveem K, Bjerve KS.
    Genet Test; 2002 Nov; 6(1):59-62. PubMed ID: 12180078
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  • 16. Analysis of HFE gene mutations (C282Y, H63D, and S65C) in the Ecuadorian population.
    Leone PE, Giménez P, Collantes JC, Paz-y-Miño C.
    Ann Hematol; 2005 Feb; 84(2):103-5. PubMed ID: 15517265
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  • 17. [Mutations in the HFE gene (C282Y, H63D, S65C) in alcoholic patients with finding of iron overload].
    Campos Franco J, González Quintela A, Fernández de Trocóniz LL, Barros Angueira F, Pérez-Quintela BV, Pérez Becerra E, Martínez de Rituerto ST, Otero Antón E, Torre Carballada JA.
    Rev Clin Esp; 2002 Oct; 202(10):534-9. PubMed ID: 12361551
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  • 18. HFE gene mutations analysis in Basque hereditary haemochromatosis patients and controls.
    de Juan D, Reta A, Castiella A, Pozueta J, Prada A, Cuadrado E.
    Eur J Hum Genet; 2001 Dec; 9(12):961-4. PubMed ID: 11840200
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  • 19. The role of HFE mutations on iron metabolism in beta-thalassemia carriers.
    Martins R, Picanço I, Fonseca A, Ferreira L, Rodrigues O, Coelho M, Seixas T, Miranda A, Nunes B, Costa L, Romão L, Faustino P.
    J Hum Genet; 2004 Dec; 49(12):651-655. PubMed ID: 15538648
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  • 20. Hereditary hemochromatosis: mutations in genes involved in iron homeostasis in Brazilian patients.
    Santos PC, Cançado RD, Pereira AC, Schettert IT, Soares RA, Pagliusi RA, Hirata RD, Hirata MH, Teixeira AC, Figueiredo MS, Chiattone CS, Krieger JE, Guerra-Shinohara EM.
    Blood Cells Mol Dis; 2011 Apr 15; 46(4):302-7. PubMed ID: 21411349
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