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Reagents, Molecular Assay, Gene Anomaly, Mutation, HJV

Definition : Molecular assay reagents intended to identify mutations in the hemojuvelin (HJV) gene, located at chromosome 1q21, which encodes instructions for producing a hemojuvelin protein that helps to regulate iron metabolism. Mutations at this locus have been identified in most adult patients with early-onset juvenile hemochromatosis.

Entry Terms : "HJV-Related Juvenile Hemochromatosis Gene Mutation Detection Reagents" , "Hemochromatosis Type 2 Gene Mutation Detection Reagents" , "Juvenile Hemochromatosis Gene Mutation Detection Reagents" , "Hemochromatosis Gene Mutation Detection Reagents" , "HJV Gene Mutation Detection Reagents" , "Hemochromatosis Diagnostic Reagents" , "Reagents, Molecular Assay, Inborn Disorder, Monogenic, Hemochromatosis"

UMDC code : 24469

   

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