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Diagnosis and management of haemochromatosis since the discovery of the HFE gene: A European experience

Robson, KJH; Merryweather-Clark, AT; Pointon, JJ; Shearman, JD; Halsall, DJ; Kelly, A; Cox, TM; (2000) Diagnosis and management of haemochromatosis since the discovery of the HFE gene: A European experience. BRITISH JOURNAL OF HAEMATOLOGY , 108 (1) pp. 31-39.

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Type: Article
Title: Diagnosis and management of haemochromatosis since the discovery of the HFE gene: A European experience
Keywords: Science & Technology, Life Sciences & Biomedicine, Hematology, HEMATOLOGY, hereditary haemochromatosis, HFE, C282Y, H63D, CELL-SURFACE EXPRESSION, PORPHYRIA-CUTANEA-TARDA, HEREDITARY HEMOCHROMATOSIS, HLA-H, CYS282TYR MUTATION, H63D MUTATIONS, C282Y MUTATION, ETHNIC-GROUPS, BLOOD-DONORS, PREVALENCE
UCL classification: UCL > School of Life and Medical Sciences
UCL > School of Life and Medical Sciences > Faculty of Medical Sciences
URI: http://discovery.ucl.ac.uk/id/eprint/25417
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