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Homozygous type 2N R854W von Willebrand factor is poorly secreted and causes a severe von Willebrand disease phenotype

✍ Scribed by G. CASTAMAN; S. H. GIACOMELLI; P. JACOBI; T. OBSER; U. BUDDE; F. RODEGHIERO; S. L. HABERICHTER; R. SCHNEPPENHEIM

Book ID: 109154428
Publisher: John Wiley and Sons
Year: 2010
Tongue: English
Weight: 231 KB
Volume: 8
Category: Article
ISSN: 1538-7933
DOI: 10.1111/j.1538-7836.2010.03971.x

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