Clinical haemochromatosis in HFE mutation carriers
- 1 August 2002
- journal article
- Published by Elsevier in The Lancet
- Vol. 360 (9330) , 411-412
- https://doi.org/10.1016/s0140-6736(02)09581-8
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- Penetrance of 845G→A (C282Y) HFE hereditary haemochromatosis mutation in the USAThe Lancet, 2002
- Prevalence of hereditary haemochromatosis in late-onset type 1 diabetes mellitus: a retrospective studyThe Lancet, 2001
- EASL International Consensus Conference on HaemochromatosisJournal of Hepatology, 2000
- Noninvasive prediction of fibrosis in C282Y homozygous hemochromatosisGastroenterology, 1998