Genetic polymorphisms on the factor V gene in women with recurrent miscarriage and acquired APCR
Author(s) -
F. Dawood,
R. Mountford,
R. G. Farquharson,
Siobhan Quenby
Publication year - 2007
Publication title -
human reproduction
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.446
H-Index - 226
eISSN - 1460-2350
pISSN - 0268-1161
DOI - 10.1093/humrep/dem210
Subject(s) - single nucleotide polymorphism , thrombophilia , factor v , recurrent miscarriage , genetics , activated protein c resistance , miscarriage , biology , medicine , factor v leiden , gene , genotype , pregnancy , thrombosis , venous thrombosis
Recurrent miscarriage (RM) has been associated with the thrombophilia, activated protein C resistance (APCR). The factor V Leiden mutation located on the B domain of the factor V gene, causes 95% of APCR and since the B domain is pivotal to APCR, it seemed plausible that other mutations or polymorphisms affecting this active domain may instigate acquired APCR. The objective of this study was to determine whether other polymorphisms exist on the parts of the gene encoding the B domain of the factor V in women with acquired APCR and RM.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom