Haemochromatosis: a gene at last?

Author:

Robson K J,Shearman J D,Merryweather-Clarke A T,Pointon J J,Rosenberg W M,Walker A P,Dooley J S,Bomford A,Raha-Chowdhury R,Worwood M

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference23 articles.

1. Association of HLA-A3 and HLA-B14 antigens with idiopathic haemochromatosis;Simon, M.; Bourel, M.; Fauchet, R.; Genetet, B.;Gut,1976

2. A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis;Feder, J.N.; Gnirke, A.; Thomas, W.;Nat Genet,1996

3. Idiopathic haemochromatosis, an iron storage disease;Finch, S.C.; Finch, C.A.;Medicine,1955

4. Prevalence of haemochromatosis amongst asymptomatic Australians;Leggett, B.A.; Halliday, J.W.; Brown, N.N.; Bryant, S.; Powell, L.W.;BrJ Haematol,1990

5. Long-term survival in patients with hereditary hemochromatosis;Niederau, C.; Fischer, R.; Purschel, A.;Gastroenterolog.y,1996

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