Polymorphic variation within the VWF gene contributes to the failure to detect mutations in patients historically diagnosed with type 1 von Willebrand disease from the MCMDM-1VWD cohort期刊界 All Journals 搜尽天下杂志传播学术成果专业期刊搜索期刊信息化学术搜索

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Polymorphic variation within the VWF gene contributes to the failure to detect mutations in patients historically diagnosed with type 1 von Willebrand disease from the MCMDM-1VWD cohort

Authors:	Daniel J Hampshire George J Burghel Jenny Goudemand Laura C S Bouvet Jeroen C J Eikenboom Reinhard Schneppenheim Ulrich Budde Ian R Peake and Anne C Goodeve

Abstract:

Keywords:	mutation single nucleotide polymorphism von Willebrand disease von Willebrand factor VWF-FVIII binding defect