Functional Characterization of Three VWF-A1 Domain Mutations Causing Type 2 Von Willebrand Disease.

M Othman, R Chegeni, LM Vickars, EJ Favaloro, D Lillicrap

Research output: Contribution to journalMeeting Abstractpeer-review

Original languageEnglish
Pages (from-to)534-535
Number of pages2
JournalBlood
Volume114
Issue number22
Publication statusPublished - 20 Nov 2009

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