Clinical haemochromatosis in HFE mutation carriers
- 1 August 2002
- journal article
- other
- Published by Elsevier in The Lancet
- Vol. 360 (9330) , 412-413
- https://doi.org/10.1016/s0140-6736(02)09583-1
Abstract
No abstract availableKeywords
This publication has 3 references indexed in Scilit:
- Penetrance of 845G→A (C282Y) HFE hereditary haemochromatosis mutation in the USAThe Lancet, 2002
- A survey of 2,851 patients with hemochromatosis:The American Journal of Medicine, 1999
- Should we genetically test everyone for haemochromatosis?Journal of Medical Ethics, 1999