Mutations C1157F and C1234W of von Willebrand factor cause intracellular retention with defective multimerization and secretion
- 1 January 2006
- journal article
- Published by Elsevier BV in Journal of Thrombosis and Haemostasis
- Vol. 4 (1), 148-157
- https://doi.org/10.1111/j.1538-7836.2005.01652.x
Abstract
No abstract availableKeywords
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