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...

Полное описание

Библиографические подробности
Главные авторы: Bastin, J, Jones, M, O'Callaghan, C, Schimanski, L, Mason, D, Townsend, A
Формат: Journal article
Язык:English
Опубликовано: 1998