This assay detects the recurring intron 1 and intron 22 inversions in the F8 gene that account for nearly half of all severe hemophilia A cases. The assay is useful for identifying the disease-causing mutation in males with severe hemophilia A, or for determining the carrier status in females with a family history of F8 intron inversions.
Transport Temperature: Ship room temperature
Reported (Analytical Time)
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