DOI:
10.1055/s-00035024
Thrombosis and Haemostasis
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References
Gu J, Jorieux S, Lavergne JM, Ruan C, Mazurier C, Meyer D.
A patient with type 2N von Willebrand disease is heterozygous for a new mutation: Gly22Glu. Demonstration of a defective expression of the second allele by the use of monoclonal antibodies.
Blood 1997;
89: 3263-9.
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