Homozygous gene conversion in von Willebrand factor gene as a cause of type 3 von Willebrand disease and predisposition to inhibitor development
Surdhar, Gurcharan K., Enayat, Mohammad S., Lawson, Sarah, Williams, Michael D., Hill, Frank G.H.
Published in Blood (01.07.2001)
Published in Blood (01.07.2001)
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Journal Article
Aberrant dimerization of von Willebrand factor as the result of mutations in the carboxy-terminal region: identification of 3 mutations in members of 3 different families with type 2A (phenotype IID) von Willebrand disease
Enayat, M. Said, Guilliatt, Andrea M., Surdhar, Gurcharan K., Jenkins, P. Vincent, Pasi, K. John, Toh, Cheng Hock, Williams, Michael D., Hill, Frank G.H.
Published in Blood (01.08.2001)
Published in Blood (01.08.2001)
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Journal Article