Identification of hereditary hemochromatosis pedigrees and a novel SLC40A1 mutation in Chinese population
Author:
Funder
The National Natural Science Foundation of China
Fundamental Research Funds
Publisher
Elsevier BV
Subject
Cell Biology,Hematology,Molecular Biology,Molecular Medicine
Reference8 articles.
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3. Mutations in HFE2 cause iron overload in chromosome 1q–linked juvenile hemochromatosis;Papanikolaou;Nat. Genet.,2003
4. Mutant antimicrobial peptide hepcidin is associated with severe juvenile hemochromatosis;Roetto;Nat. Genet.,2002
5. The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22;Camaschella;Nat. Genet.,2000
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