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IntroductionAt present, many methods are available for the genetic diagnosis of haemophilia, including indirect linkage analysis, direct sequencing. However, these methods are time‐consuming, labourious, and limited in their application. Therefore, the development of new, more effective techniques is necessary.
AimTo detect the F8 and F9 gene mutations in patients with haemophilia and their female...
IntroductionInhibitor development is a severe complication of factor IX substitution treatment for haemophilia B (HB). Current research examined the association between inhibitor development and F9 genotypes and polymorphisms in immune response genes in Chinese HB patients.
Materials and Methods11 inhibitor‐positive HB patients and 41 inhibitor‐negative HB patients were enrolled. Direct sequencing,...
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