Congenital Abnormality of the Prothrombin Molecule (Factor II) in Four Siblings: Prothrombin Barcelona
                    
                        
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                    چکیده
منابع مشابه
Congenital abnormality of the prothrombin molecule (factor II) in four siblings: prothrombin Barcelona.
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Prothrombin Molise: a "new" congenital dysprothrombinemia, double heterozygosis with an abnormal prothrombin and "true" prothrombin deficiency.
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Background & Aims:Thromboembolism is an acute cardiovascular disease that ranges from clinically unimportant to massive embolism. Both acquired and hereditary risk factors contribute to the disease. We aimed to determine the prevalence of two hereditary predisposing factor of the disease, prothrombin G20210A and factor V Leiden (G1691A) polymorphisms, in Kerman population.<br /...
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ژورنال
عنوان ژورنال: Blood
سال: 1971
ISSN: 0006-4971,1528-0020
DOI: 10.1182/blood.v38.1.9.9