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A valine deletion of ferroportin 1: a common mutation in hemochromastosis type 4.
PMID: 12123233 [PubMed - indexed for MEDLINE]
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Cited by 10 PubMed Central articles
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SLC40A1 Q248H allele frequencies and Q248H-associated risk of non-HFE iron overload in persons of sub-Saharan African descent.
Barton JC, Acton RT, Lee PL, West C.
Blood Cells Mol Dis. 2007 Sep-Oct; 39(2):206-11. Epub 2007 May 9.
[Blood Cells Mol Dis. 2007]
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The molecular basis of ferroportin-linked hemochromatosis.
De Domenico I, Ward DM, Nemeth E, Vaughn MB, Musci G, Ganz T, Kaplan J.
Proc Natl Acad Sci U S A. 2005 Jun 21; 102(25):8955-60. Epub 2005 Jun 13.
[Proc Natl Acad Sci U S A. 2005]
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Ferroportin disease due to the A77D mutation in Australia.
Subramaniam VN, Wallace DF, Dixon JL, Fletcher LM, Crawford DH.
Gut. 2005 Jul; 54(7):1048-9.
[Gut. 2005]
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