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Updated: Aug 24, 2026

Two Methods of Heterokaryon Formation to Discover HCV Restriction Factors
Published on: July 16, 2012
Identification of a novel mutation (C321X) in HJV
Franklin W Huang1, Isabel Rubio-Aliaga, James P Kushner
1Division of Medical Sciences, Harvard University, Boston, MA, USA.
Abstract:
Juvenile hemochromatosis is a rare autosomal recessive disorder characterized by the early onset of severe iron overload. We report the occurrence of compound heterozygous mutations in hemojuvelin (HJV), including a termination codon, in a patient with juvenile hemochromatosis but no family history of iron disorders.
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