Genetic hemochromatosis: Pathophysiology, diagnostic and therapeutic management
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference51 articles.
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3. The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22;Camaschella;Nat Genet,2000
4. A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis;Njajou;Nat Genet,2001
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