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...

Πλήρης περιγραφή

Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς:	Bastin, J, Jones, M, O'Callaghan, C, Schimanski, L, Mason, D, Townsend, A
Μορφή:	Journal article
Γλώσσα:	English
Έκδοση:	1998

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

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

Παρόμοια τεκμήρια