Type 2N von Willebrand disease due to Arg91Gln substitution and a cytosine deletion in exon 18 of the von Willebrand factor gene
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2141.1998.00940.x/fullpdf
Cited by 12 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
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3. Type 2N von Willebrand disease: Characterization and diagnostic difficulties;Haemophilia;2017-11-08
4. von Willebrand disease type1/type 2N compound heterozygotes: diagnostic and management challenges;British Journal of Haematology;2016-03-11
5. Biosynthesis and Organization of von Willebrand Factor;Von Willebrand Disease;2011-03-21
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