Clinical haemochromatosis in HFE mutation carriers
- PMID: 12241805
- DOI: 10.1016/s0140-6736(02)09583-1
Clinical haemochromatosis in HFE mutation carriers
Comment on
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Penetrance of 845G--> A (C282Y) HFE hereditary haemochromatosis mutation in the USA.Lancet. 2002 Jan 19;359(9302):211-8. doi: 10.1016/S0140-6736(02)07447-0. Lancet. 2002. PMID: 11812557
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