Zusammenfassung
Der von Willebrand-Faktor ist ein multimeres Glykoprotein, welches in der Hämostase zwei wichtige Funktionen erfüllt. Einerseits wird er zur Anlagerung der Plättchen an geschädigtes Endothel benötigt, andererseits bindet er sich an Gerinnungsfaktor VIII und stabilisiert diesen in der Zirkulation [1, 2]. Die Rezeptoren des von Willebrand-Faktors an der Plättchenoberfläche sind bekannt — es handelt sich dabei um die Plättchenglykoproteine Ib und IIb/IIIa [3, 4].
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© 1990 Springer-Verlag Berlin Heidelberg
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Mannhalter, C., Parzer, S., Kyrle, P.A. (1990). Molekulargenetische Untersuchungen beim yon Willebrand-Syndrom. In: Landbeck, G., Marx, R., Scharrer, I., Schramm, W. (eds) 20. Hämophilie-Symposion Hamburg 1989. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-75923-9_24
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DOI: https://doi.org/10.1007/978-3-642-75923-9_24
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