Title : Juvenile hemochromatosis associated with pathogenic mutations of adult hemochromatosis genes.

Pub. Date : 2005 Feb

PMID : 15685557






1 Functional Relationships(s)
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1 BACKGROUND AND AIMS: Juvenile hemochromatosis is a severe form of hereditary iron overload that has thus far been linked to pathogenic mutations of the gene coding for hemojuvelin (HJV), on chromosome 1, or, more rarely, that coding for hepcidin ( HAMP ), on chromosome 19. Iron hemojuvelin BMP co-receptor Homo sapiens