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Abstract
Hemophilia A (HA) is a common X-linked recessive bleeding disease caused by mutations
in FVIII gene. The identification of mutation in HA subjects can lead to more accurate
diagnosis and contribute to the genetic counseling/prenatal diagnosis.
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State Key Laboratory of Experimental Hematology, Department of Thrombosis and Hemostasis,
Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences
& Peking Union Medical College, Tianjin, China.