Inherited genetic markers for thrombophilia in northeastern Iran

  • Azimi - Nezhad
  • Published 2015

Abstract

Objective Thrombophilia is a main predisposition to thrombosis due to its procoagulant state. Several point mutations play key roles in blood-clotting disorders, which are grouped under the term thrombophilia. These thrombophilic mutations are methylenetetrahydrofolate reductase (MTHFR, C677T, and A1298C), factor V Leiden (G1691A), prothrombin gene mutation… (More)

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Cite this paper

@inproceedings{Nezhad2015InheritedGM, title={Inherited genetic markers for thrombophilia in northeastern Iran}, author={Azimi - Nezhad}, year={2015} }