المختبرات الطبية الأولى

:Normal range

Normal: absence of any detectable mutations

Carrier status: detection of a single mutation

Hereditary Hemochromatosis or a genetic predisposition to develop the disease: detection of two mutations

(Comment: The assay covers 3 most common mutations in the HFE gene (H63D, S65C, C282Y

Sample: EDTA, whole blood