Abstract
The relationship between genetic polymorphisms and migraine as a cause of an increased risk of thrombotic disorders development is still debatedIn this respect, factor V Leiden, factor V (H1299R), prothrombin G20210A, factor XIII (V34L), β-fibrinogen, MTHFR (C677T), MTHFR (A1298C), APO E, PAI-1, HPA-1 and ACE I/D seem to play a determinant role in vascular diseases related to migraine.The present review analyzes both the incidence of the above genetic vascular mutations in migraineurs and the most re-cent developments related to genetic polymorphisms and migraine.
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CITATION STYLE
Pizza, V., Agresta, A., Agresta, A., Lamaida, E., Lamaida, N., Infante, F., & Capasso, A. (2012). Migraine and Genetic Polymorphisms: An Overview. The Open Neurology Journal, 06(1), 65–70. https://doi.org/10.2174/1874205x01206010065
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