Localization of iron transport and regulatory proteins in human cells
Author:
Publisher
Oxford University Press (OUP)
Subject
General Medicine
Link
http://academic.oup.com/qjmed/article-pdf/93/9/575/
Reference22 articles.
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3. Parkkila S, Waheed A, Britton RS, et al. Immunohistochemistry of HLA‐H, the protein defective in patients with hereditary hemochromatosis, reveals unique pattern of expression in gastrointestinal tract. Proc Natl Acad Sci USA1997; 94:2534–9.
4. Feder JN, Tsuchihashi Z, Irrinki A, et al. The hemochromatosis founder mutation in HLA‐H disrupts beta2‐microglobulin interaction and cell surface expression. J Biol Chem1997; 272:14025–8.
5. Feder JN, Penny DM, Irrinki A, et al. The hemochromatosis gene product complexes with the transferrin receptor and lowers its affinity for ligand binding. Proc Natl Acad Sci USA1998; 95:1472–7.
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