A Primer for Predicting Risk of Disease inHFE-Linked Hemochromatosis
Author:
Affiliation:
1. University of Western Ontario, London, Ontario, Canada N6A 5A5
2. University of California, Irvine, CA 92697
3. University of Alabama at Birmingham, Birmingham, AL 35294-0021
Publisher
Mary Ann Liebert Inc
Subject
Genetics (clinical)
Link
http://www.liebertpub.com/doi/pdf/10.1089/109065701753617444
Reference27 articles.
1. Population screening for haemochromatosis
2. Population screening for hemochromatosis: A comparison of unbound iron-binding capacity, transferrin saturation, and C282Y genotyping in 5,211 voluntary blood donors
3. Variable phenotypic presentation of iron overload in H63D homozygotes: are genetic modifiers the cause?
4. Screening for Hemochromatosis: High Prevalence and Low Morbidity in an Unselected Population of 65,238 Persons
5. Inheritance of two HFE mutations in African Americans: Cases with hemochromatosis phenotypes and estimates of hemochromatosis phenotype frequency
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1. HFE Gene Mutations and Iron Status in 100 Healthy Polish Children;Journal of Pediatric Hematology/Oncology;2017-07
2. Reduction of Skeletal Muscle Power in Adolescent Males Carrying H63D Mutation in theHFEGene;BioMed Research International;2017
3. The impact of H63D HFE gene carriage on hemoglobin and iron status in children;Annals of Hematology;2016-08-24
4. Hemochromatosis;Yamada' s Textbook of Gastroenterology;2015-11-27
5. Hemochromatosis;Zakim and Boyer's Hepatology;2012
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