Functional consequences of ferroportin 1 mutations
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Hematology,Molecular Biology,Molecular Medicine
Reference34 articles.
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3. A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis;Njajou;Nat. Genet.,2001
4. Autosomal dominant reticuloendothelial iron overload associated with a 3-base pair deletion in the ferroportin 1 gene (SLC11A3);Devalia;Blood,2002
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