scholarly article | Q13442814 |
P356 | DOI | 10.1111/JTH.13357 |
P8608 | Fatcat ID | release_p4xdvimh45h7rpyceno745ssba |
P698 | PubMed publication ID | 27170580 |
P2093 | author name string | F Bernardi | |
P2860 | cites work | Familial thrombophilia due to a previously unrecognized mechanism characterized by poor anticoagulant response to activated protein C: prediction of a cofactor to activated protein C | Q24563608 |
Mutation in blood coagulation factor V associated with resistance to activated protein C. | Q34340007 | ||
Three novel variants in the coagulation factor V gene associated with deep venous thrombosis in Chilean patients with Amerindian ethnic background | Q41454876 | ||
A novel mutation (g2172-->c) in the factor V gene in a Chinese family with hereditary activated protein C resistance | Q43123012 | ||
Common susceptibility alleles are unlikely to contribute as strongly as the FV and ABO loci to VTE risk: results from a GWAS approach. | Q51773327 | ||
Identification and functional characterization of a novel F5 mutation (Ala512Val, FVB onn ) associated with activated protein C resistance. | Q52874413 | ||
Novel FV mutation (W1920R, FVNara) associated with serious deep vein thrombosis and more potent APC resistance relative to FVLeiden. | Q53066786 | ||
An underestimated combination of opposites resulting in enhanced thrombotic tendency. | Q53854498 | ||
P433 | issue | 7 | |
P304 | page(s) | 1350-1352 | |
P577 | publication date | 2016-06-22 | |
P1433 | published in | Journal of Thrombosis and Haemostasis | Q6296004 |
P1476 | title | Better or worse than the original. | |
P478 | volume | 14 |
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