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HJV gene mutations in European patients with juvenile hemochromatosis

22 Feb 2005

Abstract excerpt

A large variety of mutations within the genes encoding hepcidin (HAMP) and hemojuvelin (HJV) have been identified in patients with the severe iron overload disorder juvenile hemochromatosis (JH). The aim of the present study was to evaluate the molecular background of JH in patients from central parts of Europe. Sequence analyses of HAMP and HJV were performed in seven JH patients from six families from Germany,...

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PMID: 15811010
DOI: 10.1111/j.1399-0004.2005.00413.x

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