Clinical haemochromatosis in HFE mutation carriers
- 1 August 2002
- journal article
- editorial
- Published by Elsevier in The Lancet
- Vol. 360 (9330), 412-4
- https://doi.org/10.1016/s0140-6736(02)09582-x
Abstract
No abstract availableThis publication has 3 references indexed in Scilit:
- Penetrance of 845G→A (C282Y) HFE hereditary haemochromatosis mutation in the USAThe Lancet, 2002
- HFE mutations, iron deficiency and overload in 10 500 blood donorsBritish Journal of Haematology, 2001
- The effect of HFE mutations on serum ferritin and transferrin saturation in the Jersey populationBritish Journal of Haematology, 1998