Hereditary Hemochromatosis: The Clinical Significance of the S65C Mutation
Author:
Affiliation:
1. Department of Clinical Chemistry, Trondheim University Hospital, Trondheim, Norway
2. Department of Medicine, Innherred Hospital, Levanger, Norway
Publisher
Mary Ann Liebert Inc
Subject
Genetics (clinical)
Link
http://www.liebertpub.com/doi/pdf/10.1089/109065702760093933
Reference10 articles.
1. EASL International Consensus Conference on Haemochromatosis
2. HFE S65C Variant Is Not Associated with Increased Transferrin Saturation in Voluntary Blood Donors
3. Screening for Hemochromatosis: High Prevalence and Low Morbidity in an Unselected Population of 65,238 Persons
4. Commentary on HFE S65C Variant Is Not Associated with Increased Transferrin Saturation in Voluntary Blood Donors by Naveen Arya, Subrata Chakrabrati, Robert A. Hegele, Paul C. Adams
5. The Effect of HFE Genotypes on Measurements of Iron Overload in Patients Attending a Health Appraisal Clinic
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