Mutations C1157F and C1234W of von Willebrand factor cause intracellular retention with defective multimerization and secretion

Publisher： John Wiley & Sons Inc

E-ISSN： 1538-7836|4|1|148-157

ISSN： 1538-7933

Source： JOURNAL OF THROMBOSIS AND HAEMOSTASIS, Vol.4, Iss.1, 2006-01, pp. : 148-157

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