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Scandinavian Journal of Clinical and Laboratory Investigation Volume 62, 2002 - Issue 7
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Research Article

HFE mutations and hemochromatosis in Danish patients admitted for HFE genotyping

P. Koefoed Departments of Clinical Biochemistry, Clinical Pharmacology and Hepatology, Rigshospitalet, Copenhagen, Denmark; Institute of Forensic Medicine, University of Copenhagen, Denmark;
,
K. Dalhoff Departments of Clinical Biochemistry, Clinical Pharmacology and Hepatology, Rigshospitalet, Copenhagen, Denmark; Institute of Forensic Medicine, University of Copenhagen, Denmark;
,
J. Dissing Departments of Clinical Biochemistry, Clinical Pharmacology and Hepatology, Rigshospitalet, Copenhagen, Denmark; Institute of Forensic Medicine, University of Copenhagen, Denmark;
,
I. Kramer Departments of Clinical Biochemistry, Clinical Pharmacology and Hepatology, Rigshospitalet, Copenhagen, Denmark; Institute of Forensic Medicine, University of Copenhagen, Denmark;
,
N. Milman Department of Medicine, Nastved Hospital, Nastved, Denmark; Department of Pathology, Hvidovre Hospital, Hvidovre, Denmark
,
P. Pedersen Departments of Clinical Biochemistry, Clinical Pharmacology and Hepatology, Rigshospitalet, Copenhagen, Denmark; Institute of Forensic Medicine, University of Copenhagen, Denmark;
,
K. Simonsen Department of Medicine, Nastved Hospital, Nastved, Denmark; Department of Pathology, Hvidovre Hospital, Hvidovre, Denmark
,
N. Tugstrup Departments of Clinical Biochemistry, Clinical Pharmacology and Hepatology, Rigshospitalet, Copenhagen, Denmark; Institute of Forensic Medicine, University of Copenhagen, Denmark;
&
F. C. Nielsen Department of Medicine, Nastved Hospital, Nastved, Denmark; Department of Pathology, Hvidovre Hospital, Hvidovre, Denmark
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Pages 527-535 | Published online: 08 Jul 2009

Citations (6)

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Read on this site (1)

Rikke Therkildsen, Eva Efsen Dahl & Frank Vinholt Schiødt. (2022) Hereditary hemochromatosis: data from a single center Copenhagen cohort. Scandinavian Journal of Gastroenterology 57:8, pages 972-977.
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Articles from other publishers (5)

Palle Pedersen, Gitte Vedel Melsen & Nils Milman. (2008) Frequencies of the haemochromatosis gene (HFE) variants C282Y, H63D and S65C in 6,020 ethnic Danish men. Annals of Hematology 87:9, pages 735-740.
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Jónrit Halling, Maria Skaalum Petersen, Philippe Grandjean, Pál Weihe & Kim Brosen. (2008) Genetic predisposition to Parkinson's disease: CYP2D6 and HFE in the Faroe Islands. Pharmacogenetics and Genomics 18:3, pages 209-212.
Crossref
Mark Worwood. (2005) Inherited iron loading: genetic testing in diagnosis and management. Blood Reviews 19:2, pages 69-88.
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Nils Milman, Torkil á Steig, Pernille Koefoed, Palle Pedersen, Kirsten Fenger & Finn Cilius Nielsen. (2004) Frequency of the hemochromatosis HFE mutations C282Y, H63D, and S65C in blood donors in the Faroe Islands. Annals of Hematology 84:3, pages 146-149.
Crossref
Nils Milman, Pernille Koefoed, Palle Pedersen, Finn Cilius Nielsen & Hans Eiberg. (2003) Frequency of the HFE C282Y and H63D mutations in Danish patients with clinical haemochromatosis initially diagnosed by phenotypic methods . European Journal of Haematology 71:6, pages 403-407.
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