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

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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Detalles Bibliográficos
Autores principales:	Bastin, J, Jones, M, O'Callaghan, C, Schimanski, L, Mason, D, Townsend, A
Formato:	Journal article
Lenguaje:	English
Publicado:	1998

Kupffer cell staining by an HFE-specific monoclonal antibody: implications for hereditary haemochromatosis por Bastin, J, Jones, M, O'Callaghan, C, Schimanski, L, Mason, D, Townsend, A

Publicado 1998

Journal article

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 por Bastin, J, Jones, M, O'Callaghan, C, Schimanski, L, Mason, D, Townsend, A

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