HEMOCHROMATOSIS MUTATION DETECTION (C282Y, H63D, & S65C), HEREDITARY
Hereditary hemochromatosis is an autosomal recessive disorder of iron metabolism.
Specimen Collection Requirements
Whole Blood, one 3 mL lavender (EDTA), pink (K2EDTA) or yellow (ACD Solution A or B) top tube
Serum, plasma, frozen whole blood, clotted blood and severely hemolyzed samples
Ambient: 3 days; Refrigerated: 1 week; Frozen: Unacceptable
Polymerase Chain Reaction/Fluorescence Monitoring
Thursday, January 5, 2017 03:42:15 AM