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Journal Abstract Search

115 related items for PubMed ID: 15749661

  • 1. Two novel mutations, L490R and V561X, of the transferrin receptor 2 gene in Japanese patients with hemochromatosis.
    Koyama C, Wakusawa S, Hayashi H, Suzuki R, Yano M, Yoshioka K, Kozuru M, Takayamam Y, Okada T, Mabuchi H.
    Haematologica; 2005 Mar; 90(3):302-7. PubMed ID: 15749661
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  • 2. Two novel mutations, L490R and V561X, in transferrin receptor 2 in Japanese patients with hemochromatosis.
    Bergamaschi G.
    Haematologica; 2005 Mar; 90(3):289A. PubMed ID: 15749651
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  • 3. Homozygous p.M172K mutation of the TFR2 gene in an Italian family with type 3 hereditary hemochromatosis and early onset iron overload.
    Majore S, Milano F, Binni F, Stuppia L, Cerrone A, Tafuri A, De Bernardo C, Palka G, Grammatico P.
    Haematologica; 2006 Aug; 91(8 Suppl):ECR33. PubMed ID: 16923517
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  • 4. Early onset hereditary hemochromatosis resulting from a novel TFR2 gene nonsense mutation (R105X) in two siblings of north French descent.
    Le Gac G, Mons F, Jacolot S, Scotet V, Férec C, Frébourg T.
    Br J Haematol; 2004 Jun; 125(5):674-8. PubMed ID: 15147384
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  • 9. AVAQ 594-597 deletion of the TfR2 gene in a Japanese family with hemochromatosis.
    Hattori A, Wakusawa S, Hayashi H, Harashima A, Sanae F, Kawanaka M, Yamada G, Yano M, Yoshioka K.
    Hepatol Res; 2003 Jun; 26(2):154-156. PubMed ID: 12809944
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  • 10. Hemochromatosis due to mutations in transferrin receptor 2.
    Roetto A, Daraio F, Alberti F, Porporato P, Calì A, De Gobbi M, Camaschella C.
    Blood Cells Mol Dis; 2002 Jun; 29(3):465-70. PubMed ID: 12547237
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  • 11. Population-based study of the relationship between mutations in the hemochromatosis (HFE) gene and arthritis.
    Sherrington CA, Knuiman MW, Divitini ML, Bartholomew HC, Cullen DJ, Olynyk JK.
    J Gastroenterol Hepatol; 2006 Mar; 21(3):595-8. PubMed ID: 16638105
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  • 15. H63D homozygotes with hyperferritinaemia: Is this genotype, the primary cause of iron overload?
    de Diego C, Opazo S, Murga MJ, Martínez-Castro P.
    Eur J Haematol; 2007 Jan; 78(1):66-71. PubMed ID: 17042772
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  • 17. Searching for hereditary hemochromatosis.
    Laudicina RJ.
    Clin Lab Sci; 2006 Jan; 19(3):174-83. PubMed ID: 16910235
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