Method for the identification of a risk for a thrombogenic disorder by determining the TAFI-lle347 polymorphism

The present invention is directed to a method identifying a risk for a thrombogenic disorder including, without limitation, atrial fibrillation, stroke, prolonged intermitted neurological deficit (PRIND), transitory ischemic attack (TIA), atherosclerotic cerebrovascular disease (CVD) and/or coronary...

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Bibliographische Detailangaben
Hauptverfasser: SIEGLER, KARL-ERNST, DELEUZE, JEAN-FRANCOIS, SCHOELKENS, BERNWARD DR, KOZIAN, DETLEF DR, MACE, SANDRINE, RICARD, SYLVAIN, SCHAEFER, STEFAN DR
Format: Patent
Sprache:eng ; fre ; ger
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Zusammenfassung:The present invention is directed to a method identifying a risk for a thrombogenic disorder including, without limitation, atrial fibrillation, stroke, prolonged intermitted neurological deficit (PRIND), transitory ischemic attack (TIA), atherosclerotic cerebrovascular disease (CVD) and/or coronary heart disease, as well as to a method for selecting patients with a risk for a thrombogenic disorder, to a method for identifying a pharmaceutical for the therapy or prophylaxis of a thrombogenic disorder as well as to a method for producing a medicament and a diagnostic by employing the TAFI-Ile347 polymorphism.