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Article Summary

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Factor 8 (F8) gene mutation profile of Turkish hemophilia A patients with inhibitors
Blood Coagulation & Fibrinolysis, 07/10/08

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Free Abstract

Fidanci ID et al. - All mutation types detected were in agreement with the severe hemophilia A phenotype, most likely leading to a deficiency of and predisposition to the development of alloantibodies against FVIII. It is seen that Turkish hemophilia A patients with major molecular defects have a higher possibility of developing inhibitors.

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