HEMOPHILIA A, HEMOPHILIA B & VON WILLEBRAND DISEASE MUTATION DETECTION

155 Ratings

Rs 29,260 Rs 22,000

25 % OFF

HEMOPHILIA A & B REFER TO FACTOR VIII & FACTOR IX DEFICIENCY RESPECTIVELY. THEY ARE INHERITED IN AN X-LINKED RECESSIVE PATTERN. THEY ARE CAUSED BY PATHOGENIC VARIANTS DUE TO MUTATION OR DELETION IN F8 OR F9 GENE. VWD IS A BLEEDING DISORDER CAUSED BY THE DEFECT IN CHROMOSOME 12 AND CAN BE INHERITED FROM BOTH PARENTS. DETECTION OF THESE MUTATIONS FACILITATES INHIBITOR RISK PREDICTION, CARRIER DETECTION & PRENATAL DIAGNOSIS FOR AFFECTED FAMILIES.

HEMOPHILIA A, HEMOPHILIA B & VON WILLEBRAND DISEASE MUTATION DETECTION

Rs 29,260 Rs 22,000

25 % OFF

Why book with us?

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HEMOPHILIA A, HEMOPHILIA B & VON WILLEBRAND DISEASE MUTATION DETECTION

Rs 29,260 Rs 22,000

25 % OFF

Why book with us?

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