[HTML][HTML] Interaction of hemojuvelin with neogenin results in iron accumulation in human embryonic kidney 293 cells
AS Zhang, AP West, AE Wyman, PJ Bjorkman… - Journal of Biological …, 2005 - ASBMB
Type 2 hereditary hemochromatosis (HH) or juvenile hemochromatosis is an early onset,
genetically heterogeneous, autosomal recessive disorder of iron overload. Type 2A HH is
caused by mutations in the recently cloned hemojuvelin gene (HJV; also called
HFE2)(Papanikolaou, G., Samuels, ME, Ludwig, EH, MacDonald, ML, Franchini, PL, Dube,
MP, Andres, L., MacFarlane, J., Sakellaropoulos, N., Politou, M., Nemeth, E., Thompson, J.,
Risler, JK, Zaborowska, C., Babakaiff, R., Radomski, CC, Pape, TD, Davidas, O., Christakis …
genetically heterogeneous, autosomal recessive disorder of iron overload. Type 2A HH is
caused by mutations in the recently cloned hemojuvelin gene (HJV; also called
HFE2)(Papanikolaou, G., Samuels, ME, Ludwig, EH, MacDonald, ML, Franchini, PL, Dube,
MP, Andres, L., MacFarlane, J., Sakellaropoulos, N., Politou, M., Nemeth, E., Thompson, J.,
Risler, JK, Zaborowska, C., Babakaiff, R., Radomski, CC, Pape, TD, Davidas, O., Christakis …
