A novel two base pair deletion in the factor V gene associated with severe factor V deficiency-Reference-Cited by-同舟云学术

A novel two base pair deletion in the factor V gene associated with severe factor V deficiency

Published:2000-12 Issue:4 Volume:111 Page:1240-1246
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:Br J Haematol

Author:

Montefusco Maria Claudia,Duga Stefano,Asselta Rosanna,Santagostino Elena,Mancuso Giacomo,Malcovati Massimo,Mannucci Pier Mannuccio,Tenchini Maria Luisa

Publisher

Wiley

Subject

Hematology

Reference33 articles.

1. Mutation in blood coagulation factor V associated with resistance to activated protein C

2. Phenotypic homozygous activated protein C resistance associated with compound heterozygosity for Arg506Gln (factor V Leiden) and His1299Arg substitutions in factor V

3. Molecular Bases of Pseudo-homozygous APC Resistance: The Compound Heterozygosity for FV R506Q and a FV Null Mutation Results in the Exclusive Presence of FV Leiden Molecules in Plasma

4. Structure of the gene for human coagulation factor V

5. Fatal haemorrhage and incomplete block to embryogenesis in mice lacking coagulation factor V

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