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This page is a summary of: Severe factor X deficiency in three unrelated Palestinian patients is caused by homozygosity for the mutation c302delG-correlation with thrombin generation and thromboelastometry, Blood Coagulation & Fibrinolysis, December 2011, Wolters Kluwer Health,
DOI: 10.1097/mbc.0b013e32834ad785.
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