The Magnificent VWF SNPs and Where to Find Them: A Journey in Exon 28 of the Hispanic Population

Abstract von Willebrand disease (VWD) is a common coagulation disorder with a prevalence of 0.1% to 1.0% manifesting as a wide spectrum of bleeding symptoms. Type 1 is diagnosed by confirming a quantitative decrease in VWF level, while type 3 has undetectable levels of VWF. Type 2 VWD variants are c...

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Veröffentlicht in:	American journal of clinical pathology 2019-09, Vol.152 (Supplement_1), p.S16-S17
Hauptverfasser:	Barouqa, Mohammad, Choudhuri, Jui, Fecher, Roger, Jacob, Jack, Sadeghi, Saed, Gil, Morayma Reyes
Format:	Artikel
Sprache:	eng
Schlagworte:	African Americans Benign Collagen Hispanic people Polymorphism Ristocetin Single-nucleotide polymorphism Statistical analysis Von Willebrand factor
Online-Zugang:	Volltext
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