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Von Willebrand’s Disease caused by Compound Heterozygosity for a Substitution Mutation (T1156M) in the D3 Domain of the Von Willebrand Factor and a Stop Mutation (Q2470X)
Lethagen, Stefan, Isaksson, Christina, Schaedel, Charlotta, Holmberg, LarsVolume:
88
Year:
2002
Language:
english
Journal:
Thrombosis and Haemostasis
DOI:
10.1055/s-0037-1613232
File:
PDF, 157 KB
english, 2002