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Mutation analysis in the F8 gene in 485 families with haemophilia A and prenatal diagnosis in China

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Haemophilia A (HA) is an X‐linked bleeding disorder caused by mutations in the coagulation factor Ⅷ (F8) gene. Its incidence in men is estimated to be approximately 1/5000. Click to show full abstract

Haemophilia A (HA) is an X‐linked bleeding disorder caused by mutations in the coagulation factor Ⅷ (F8) gene. Its incidence in men is estimated to be approximately 1/5000.

Keywords: families haemophilia; 485 families; mutation analysis; gene 485; analysis gene; gene

Journal Title: Haemophilia
Year Published: 2020

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