In vitro binding of HFE to the cation-independent mannose-6 phosphate receptor.

Hereditary hemochromatosis is most frequently associated with mutations in HFE, which encodes a class Ib histocompatibility protein. HFE binds to the transferrin receptor-1 (TfR1) in competition with iron-loaded transferrin (Fe-Tf). HFE is released from TfR1 by increasing concentrations of Fe-Tf, an...

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Bibliographic Details
Main Authors: Schimanski, L, Drakesmith, H, Sweetland, E, Bastin, J, Rezgui, D, Edelmann, M, Kessler, B, Merryweather-Clarke, A, Robson, K, Townsend, A
Format: Journal article
Language:English
Published: 2009