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Molecular genetic analysis of factor XI deficiency: Identification of five novel gene alterations and the origin of type II mutation in Portuguese families
Journal article   Peer reviewed

Molecular genetic analysis of factor XI deficiency: Identification of five novel gene alterations and the origin of type II mutation in Portuguese families

C Ventura, AIM Santos, A Tavares, T Gago, J Lavinha, JH McVey and D David
THROMBOSIS AND HAEMOSTASIS, Vol.84(5), pp.833-840
01/11/2000

Abstract

Science & Technology Life Sciences & Biomedicine Hematology Peripheral Vascular Disease Cardiovascular System & Cardiology HEMATOLOGY PERIPHERAL VASCULAR DISEASE FXI deficiency phenotype FXI mutations FXI pre-mRNA splicing origin of the type II mutation COAGULATION-FACTOR-XI POLYMERASE CHAIN-REACTION BLOOD-COAGULATION CONFORMATION POLYMORPHISM POINT MUTATIONS ASHKENAZI JEWS DIATHESIS DEFECT SYSTEM
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