Autografting as a risk factor for persisting iron overload in long-term survivors of acute myeloid leukaemia
Author:
Publisher
Springer Science and Business Media LLC
Subject
Transplantation,Hematology
Link
http://www.nature.com/articles/1704244.pdf
Reference17 articles.
1. Feder JN, Gnirke A, Thomas W et al. A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis. Nat Genet 1996; 13: 399–408.
2. Townsend A, Drakesmith H . Role of HFE in iron metabolism, hereditary haemochromatosis, anaemia of chronic disease, and secondary iron overload. Lancet 2002; 359: 786–790.
3. Beutler E . The significance of the 187G (H63D) mutation in hemochromatosis. Am J Hum Genet 1997; 61: 762–764.
4. Worwood M . Pathogenesis and management of haemochromatosis. Br J Haematol 1999; 105 (Suppl. 1): 16–18.
5. Porter JB . Practical management of iron overload. Br J Haematol 2001; 115: 239–252.
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