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Li, V. F5 Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/5495 (accessed on 21 September 2026).
Li V. F5 Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/5495. Accessed September 21, 2026.
Li, Vivi. "F5 Gene" Encyclopedia, https://encyclopedia.pub/entry/5495 (accessed September 21, 2026).
Li, V. (2020, December 24). F5 Gene. In Encyclopedia. https://encyclopedia.pub/entry/5495
Li, Vivi. "F5 Gene." Encyclopedia. Web. 24 December, 2020.
F5 Gene
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Coagulation factor V

genes

References

  1. Asselta R, Peyvandi F. Factor V deficiency. Semin Thromb Hemost. 2009Jun;35(4):382-9. doi: 10.1055/s-0029-1225760.
  2. Asselta R, Tenchini ML, Duga S. Inherited defects of coagulation factor V: thehemorrhagic side. J Thromb Haemost. 2006 Jan;4(1):26-34. Review.
  3. Brugge JM, Simioni P, Bernardi F, Tormene D, Lunghi B, Tans G, Pagnan A,Rosing J, Castoldi E. Expression of the normal factor V allele modulates the APC resistance phenotype in heterozygous carriers of the factor V Leiden mutation. J Thromb Haemost. 2005 Dec;3(12):2695-702.
  4. Castoldi E, Rosing J. Factor V Leiden: a disorder of factor V anticoagulantfunction. Curr Opin Hematol. 2004 May;11(3):176-81. Review.
  5. Colak Y, Karasu Z, Oruc N, Can C, Balým Z, Akarca U, Gunsar F, Ersoz G, Tokat Y, Batur Y. Hyperhomocysteinaemia and factor V Leiden mutation are associatedwith Budd-Chiari syndrome. Eur J Gastroenterol Hepatol. 2006 Aug;18(8):917-20.
  6. Cutler JA, Patel R, Rangarajan S, Tait RC, Mitchell MJ. Molecularcharacterization of 11 novel mutations in patients with heterozygous andhomozygous FV deficiency. Haemophilia. 2010 Nov;16(6):937-42. doi:10.1111/j.1365-2516.2010.02330.x.
  7. Duga S, Asselta R, Tenchini ML. Coagulation factor V. Int J Biochem Cell Biol.2004 Aug;36(8):1393-9. Review.
  8. Grody WW, Griffin JH, Taylor AK, Korf BR, Heit JA; ACMG Factor V. LeidenWorking Group. American College of Medical Genetics consensus statement on factorV Leiden mutation testing. Genet Med. 2001 Mar-Apr;3(2):139-48.
  9. Janssen HL, Meinardi JR, Vleggaar FP, van Uum SH, Haagsma EB, van Der Meer FJ,van Hattum J, Chamuleau RA, Adang RP, Vandenbroucke JP, van Hoek B, Rosendaal FR.Factor V Leiden mutation, prothrombin gene mutation, and deficiencies incoagulation inhibitors associated with Budd-Chiari syndrome and portal veinthrombosis: results of a case-control study. Blood. 2000 Oct 1;96(7):2364-8.
  10. Lak M, Sharifian R, Peyvandi F, Mannucci PM. Symptoms of inherited factor Vdeficiency in 35 Iranian patients. Br J Haematol. 1998 Dec;103(4):1067-9.
  11. Mann KG, Kalafatis M. Factor V: a combination of Dr Jekyll and Mr Hyde. Blood.2003 Jan 1;101(1):20-30.
  12. Nicolaes GA, Dahlbäck B. Factor V and thrombotic disease: description of ajanus-faced protein. Arterioscler Thromb Vasc Biol. 2002 Apr 1;22(4):530-8.Review.
  13. Ornstein DL, Cushman M. Cardiology patient page. Factor V Leiden. Circulation.2003 Apr 22;107(15):e94-7.
  14. Rosendorff A, Dorfman DM. Activated protein C resistance and factor V Leiden: a review. Arch Pathol Lab Med. 2007 Jun;131(6):866-71. Review.
  15. Segers K, Dahlbäck B, Nicolaes GA. Coagulation factor V and thrombophilia:background and mechanisms. Thromb Haemost. 2007 Sep;98(3):530-42. Review.
  16. Vos HL. Inherited defects of coagulation Factor V: the thrombotic side. JThromb Haemost. 2006 Jan;4(1):35-40.
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Update Date: 24 Dec 2020
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