A method for homogeneous color-compensated genotyping of factor V (G1691A) and methylenetetrahydrofolate reductase (C677T) mutations using real-time multiplex fluorescence PCR
Author:
Publisher
Elsevier BV
Subject
Clinical Biochemistry,General Medicine
Reference19 articles.
1. Venous thrombosis;Rosendaal;Lancet,1999
2. The methylenetetrahydrofolate reductase TT677 genotype is associated with venous thrombosis independently of the coexistence of the FV Leiden and the prothrombin A20210 mutation;Margaglione;Thromb Haemost,1998
3. A common mutation in the methylenetetrahydrofolate reductase gene (C677T) increases the risk for deep-vein thrombosis in patients with mutant factor V (factor V:Q506);Cattaneo;Arterioscler Thromb Vasc Biol,1997
4. Blood coagulation;Dahlbäck;Lancet,2000
5. Rapid detection of prothrombotic mutations of prothrombin (G20210A), factor V (G1691A) and methylenetetrahydrofolate reductase (C677T) by real time fluorescence PCR with the LightCycler;von Ahsen;Clin Chem,1999
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