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January 2005 - Volume 16 - Issue 1
pp: 1-89

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

Isshiki, Ikuko; Favier, Remi; Moriki, Takanori; More

Blood Coagulation & Fibrinolysis. 16(1):9-16, January 2005.