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Comment

. 2003 Apr;52(4):610-1.

doi: 10.1136/gut.52.4.610-a.

Penetrance of haemochromatosis

PMID: 12631680
PMCID: PMC1773594
DOI: 10.1136/gut.52.4.610-a

Comment

Penetrance of haemochromatosis

E Beutler. Gut. 2003 Apr.

. 2003 Apr;52(4):610-1.

doi: 10.1136/gut.52.4.610-a.

Author

PMID: 12631680
PMCID: PMC1773594
DOI: 10.1136/gut.52.4.610-a

No abstract available

PubMed Disclaimer

Comment on

Underdiagnosis of hereditary haemochromatosis: lack of presentation or penetration?
Ryan E, Byrnes V, Coughlan B, Flanagan AM, Barrett S, O'Keane JC, Crowe J. Ryan E, et al. Gut. 2002 Jul;51(1):108-12. doi: 10.1136/gut.51.1.108. Gut. 2002. PMID: 12077102 Free PMC article.

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References

1. Beutler E, Felitti VJ, Koziol JA, et al. Penetrance of the 845G6A (C282Y) HFE hereditary haemochromatosis mutation in the USA. Lancet 2002;359:211–18. - PubMed
1. Phatak PD, Ryan DH, Cappuccio J, et al. Prevalence and penetrance of HFE mutations in 4865 unselected primary care patients. Blood Cells Mol Dis 2002;29:41–7. - PubMed
1. Asberg A, Hveem K, Kruger O, et al. Persons with screening-detected haemochromatosis: as healthy as the general population? Scand J Gastroenterol 2002;37:719–24. - PubMed
1. Waalen J, Felitti V, Gelbart T, et al. Prevalence of hemochromatosis-related symptoms in homozygotes for the C282Y mutation of the HFE gene. Mayo Clin Proc 2002;77:522–30. - PubMed
1. Jackson HA, Carter K, Darke C, et al. HFE mutations, iron deficiency and overload in 10 500 blood donors. Br J Haematol 2001;114:474–84. - PubMed

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