Search Results - "Murakami, Morika"
-
1
Congenital coagulation factor X deficiency: Genetic analysis of five patients and functional characterization of mutant factor X proteins
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-09-2018)“…Congenital factor X (FX) deficiency is a rare bleeding disorder that is inherited as an autosomal recessive trait. In this study, a genetic analysis of the FX…”
Get full text
Journal Article -
2
Gene analysis of inherited antithrombin deficiency and functional analysis of abnormal antithrombin protein (N87D)
Published in International journal of hematology (01-04-2018)“…Inherited antithrombin (AT) deficiency is one of the most clinically significant forms of congenital thrombophilia and follows an autosomal dominant mode of…”
Get full text
Journal Article