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See Latest ArticlesStudy of mutations in Jordanian patients with haemophilia A: identification of five novel mutations
Haemophilia, 10/12/09
Awidi A et al. – Haemophilia A (HA) is an X–linked recessive bleeding disorder caused by mutations in the factor VIII gene (F8), which encodes factor VIII (FVIII) protein, a plasma glycoprotein, that plays an important role in the blood coagulation cascade. In the present study, the aim was to identify F8 gene mutations in HA patients from Jordan. The data presented will play an important role for genetic counselling and health care of HA patients in Jordan.
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