Clinical haemochromatosis in HFE mutation carriers
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference5 articles.
1. Penetrance of 845G- > A (C282Y) HFE hereditary haemochromatosis mutation in the USA;Beutler;Lancet,2002
2. Practical genetic counselling;Harper,1998
3. A survey of 2,851 patients with hemochromatosis: symptoms and response to treatment;McDonnell;Am J Med,1999
4. Should we genetically test everyone for haemochromatosis?;Allen;J Med Ethics,1999
5. Screening for hereditary haemochromatosis should be implemented now;Allen;BMJ,2000
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