https://www.selleckchem.com/pr....oducts/bgj398-nvp-bg
ssential to elucidate the mechanism behind the difference between the drugs of the same class. © 2020 S. Karger AG, Basel.INTRODUCTION Congenital afibrinogenemia is a rare autosomal recessive disorder characterized by bleeding that varies from mild to severe and by complete absence or extremely low levels of plasma and platelet fibrinogen. Hypofibrinogenemia is characterized by fibrinogen levels less then 1.5 g/L. OBJECTIVE In this study, we analyzed fibrinogen beta chain gene mutations in Turkish afibrinogenemia and hypofibri
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