Genetic analysis of hereditary factor X deficiency in a French patient of Sri Lankan ancestry: In vitro expression study identified Gly366Ser substitution as the molecular basis of the dysfunctional factor X

Ikuko Isshiki, Remi Favier, Takanori Moriki, Toshihiro Uchida, Hiroaki Ishihara, Patrick Van Dreden, Mitsuru Murata, Yasuo Ikeda

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Medicine & Life Sciences