Cite
HARVARD Citation
Mitchell, M. et al. (2019). Genotype analysis and identification of novel mutations in a multicentre cohort of patients with hereditary factor X deficiency. Blood coagulation and fibrinolysis. 30 (1), p. . [Online].
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Mitchell, M. et al. (2019). Genotype analysis and identification of novel mutations in a multicentre cohort of patients with hereditary factor X deficiency. Blood coagulation and fibrinolysis. 30 (1), p. . [Online].