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. 2010 Sep;18(9).

doi: 10.1038/ejhg.2009.245. Epub 2010 Feb 3.

Clinical utility gene card for: Haemochromatosis [HFE]

Manfred Stuhrmann¹, Heinz Gabriel, Stephen Keeney

Affiliations

PMID: 20125190
PMCID: PMC2987432
DOI: 10.1038/ejhg.2009.245

Clinical utility gene card for: Haemochromatosis [HFE]

Manfred Stuhrmann et al. Eur J Hum Genet. 2010 Sep.

. 2010 Sep;18(9).

doi: 10.1038/ejhg.2009.245. Epub 2010 Feb 3.

Authors

Manfred Stuhrmann¹, Heinz Gabriel, Stephen Keeney

Affiliation

¹ Institute of Human Genetics, Medical School Hannover, Hannover, Germany. stuhrmann.manfred@mh-hannover.de

PMID: 20125190
PMCID: PMC2987432
DOI: 10.1038/ejhg.2009.245

No abstract available

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References

1. Feder JN, Gnirke A, Thomas W, et al. A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis. Nat Genet. 1996;13:399–408. - PubMed
1. Hanson EH, Imperatore G, Burke W. HFE gene and hereditary hemochromatosis: a HuGE review. Human Genome Epidemiology. Am J Epidemiol. 2001;154:193–206. - PubMed
1. Pointon JJ, Wallace D, Merryweather-Clarke AT, Robson KJ. Uncommon mutations and polymorphisms in the hemochromatosis gene. Genet Test. 2000;4:151–161. - PubMed
1. Papanikolaou G, Politou M, Terpos E, Fourlemadis S, Sakellaropoulos N, Loukopoulos D. Hereditary hemochromatosis. HFE mutation analysis in Greeks reveals genetic heterogeneity. Blood Cells Mol Dis. 2000;26:163–168. - PubMed
1. Stuhrmann M, Strassburg C, Schmidtke J. Genotype-based screening for hereditary haemochromatosis. I: Technical performance, costs and clinical relevance of a German pilot study. Eur J Hum Genet. 2005;13:69–78. - PubMed

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