Thrombotic risk according to SERPINC1 genotype in a large cohort of subjects with antithrombin inherited deficiency

Summary Inherited quantitative (type I) or qualitative (type II) antithrombin deficiency (ATD) due to mutations in the SERPINC1 gene is a well-known risk factor for venous thromboembolism. ATD may also increase risk for arterial thrombosis. Few studies have investigated risk for thrombosis according...

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Veröffentlicht in:	Thrombosis and haemostasis 2017, Vol.56 (6), p.1040-1051
Hauptverfasser:	Alhenc-Gelas, Martine, Plu-Bureau, Genevieve, Hugon-Rodin, Justine, Picard, Veronique, Horellou, Marie-Helene
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Adult Aged Aged, 80 and over Antithrombin III - genetics Arteries - pathology Child Child, Preschool Coagulation and Fibrinolysis DNA Mutational Analysis Female Genotype Humans Infant Male Middle Aged Mutation - genetics Pedigree Prevalence Prognosis Retrospective Studies Risk Thrombosis - diagnosis Thrombosis - epidemiology Thrombosis - genetics Venous Thromboembolism - diagnosis Venous Thromboembolism - epidemiology Venous Thromboembolism - genetics Young Adult
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