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.

Näytä muut versiot (1)

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...

Bibliografiset tiedot
Päätekijät:	Bastin, J, Jones, M, O'Callaghan, C, Schimanski, L, Mason, D, Townsend, A
Aineistotyyppi:	Journal article
Kieli:	English
Julkaistu:	1998

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