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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

Ventura, C, Santos, AIM, Tavares, A, Gago, T, Lavinha, J, McVey, JH and David, D (2000) Molecular genetic analysis of factor XI deficiency: Identification of five novel gene alterations and the origin of type II mutation in Portuguese families THROMBOSIS AND HAEMOSTASIS, 84 (5). pp. 833-840.

Full text not available from this repository.
Item Type: Article
Authors :
NameEmailORCID
Ventura, CUNSPECIFIEDUNSPECIFIED
Santos, AIMUNSPECIFIEDUNSPECIFIED
Tavares, AUNSPECIFIEDUNSPECIFIED
Gago, TUNSPECIFIEDUNSPECIFIED
Lavinha, JUNSPECIFIEDUNSPECIFIED
McVey, JHj.mcvey@surrey.ac.ukUNSPECIFIED
David, DUNSPECIFIEDUNSPECIFIED
Date : 1 November 2000
Uncontrolled Keywords : 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
Related URLs :
Depositing User : Symplectic Elements
Date Deposited : 17 May 2017 09:59
Last Modified : 17 May 2017 14:46
URI: http://epubs.surrey.ac.uk/id/eprint/825921

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