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Journal Abstract Search

149 related items for PubMed ID: 16521305

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  • 4. Novel human pathological mutations. Gene symbol: SLC40A1. Disease: haemochromatosis, type 4.
    Relvas L, Claro MT, Bento MC, Ribeiro ML.
    Hum Genet; 2009 Apr; 125(3):338. PubMed ID: 19309784
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  • 6. A novel mutation in ferroportin implicated in iron overload.
    Wallace DF, Dixon JL, Ramm GA, Anderson GJ, Powell LW, Subramaniam VN.
    J Hepatol; 2007 May; 46(5):921-6. PubMed ID: 17383046
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  • 7. The homozygous mutation G75R in the human SLC11A2 gene leads to microcytic anaemia and iron overload.
    Barrios M, Moreno-Carralero MI, Cuadrado-Grande N, Baro M, Vivanco JL, Morán-Jiménez MJ.
    Br J Haematol; 2012 May; 157(4):514-6. PubMed ID: 22313374
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  • 16. Gene symbol: SLC7A9. Disease: cystinuria, type non-I.
    Nunes V, Font-Llitjós M, Jiménez-Vidal M, Bisceglia L, Di Perna M, de Sanctis L, Rousaud F, Zelante L, Palacín M.
    Hum Genet; 2005 Feb; 116(3):236. PubMed ID: 15818815
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  • 18. Mutation analysis of hepcidin and ferroportin genes in Italian prospective blood donors with iron overload.
    Duca L, Delbini P, Nava I, Vaja V, Fiorelli G, Cappellini MD.
    Am J Hematol; 2009 Sep; 84(9):592-3. PubMed ID: 19610021
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  • 19. SLC40A1-R178G or R178Q and ferroportin disease? A call for vigilance in mutation reporting.
    Wallace DF.
    J Hepatol; 2013 Aug; 59(2):396-7. PubMed ID: 23523714
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  • 20. Reply to: "SLC40A1-R178G or R178Q and ferroportin disease? A call for vigilance in mutation reporting".
    Speletas M, Kioumi A, Germenis AE.
    J Hepatol; 2013 Aug; 59(2):397. PubMed ID: 23523713
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