A targeted approach significantly increases the identification rate of patients with undiagnosed haemochromatosis-Reference-Cited by-同舟云学术

A targeted approach significantly increases the identification rate of patients with undiagnosed haemochromatosis

Published:2003-02 Issue:2 Volume:253 Page:217-224
ISSN:0954-6820
Container-title:Journal of Internal Medicine
language:en
Short-container-title:J Intern Med

Author:

Cadet E.,Capron D.,Perez A. S.,Crepin S. N.,Arlot S.,Ducroix J.-P.,Dautreaux M.,Fardellone P.,Leflon P.,Merryweather-Clarke A. T.,Livesey K. J.,Pointon J. J.,Rose P.,Harcourt J.,Emery J.,Sueur J. M.,Feyt R.,Robson K. J. H.,Rochette J.

Publisher

Wiley

Subject

Internal Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2796.2003.01094.x/fullpdf

Reference32 articles.

1. Haemochromatosis and HLA–H

2. A simple genetic test identifies 90% of UK patients with haemochromatosis

3. A novel MHC class I–like gene is mutated in patients with hereditary haemochromatosis

4. Distribution of transferrin saturation in an Australian population: Relevance to the early diagnosis of hemochromatosis

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