Kupffer cell staining by an HFE-specific monoclonal antibody: implications for hereditary haemochromatosis.

Kupffer cell staining by an HFE-specific monoclonal antibody: implications for hereditary haemochromatosis.

Hiển thị phiên bản (1) khác

Hereditary haemochromatosis is an inherited disorder of iron absorption that leads to excessive iron storage in the liver and other organs. A candidate disease gene HFE has been identified that encodes a novel MHC class I like protein. We report the development of a monoclonal antibody (HFE-JB1) spe...

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Chi tiết về thư mục
Những tác giả chính:	Bastin, J, Jones, M, O'Callaghan, C, Schimanski, L, Mason, D, Townsend, A
Định dạng:	Journal article
Ngôn ngữ:	English
Được phát hành:	1998

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