Mutation analysis in the F8 gene in 485 families with haemophilia A and prenatal diagnosis in China
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DOI: 10.1111/hae.14206
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. read more here.
Keywords: families haemophilia; 485 families; mutation analysis; gene 485 ... See more keywords