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Autosomal Recessive von Willebrand Disease Type 1 or 2 due to Homozygous or Compound Heterozygous Mutations in the von Willebrand Factor Gene: A Single Center Experience on Molecular Heterogeneity and Laboratory Features in 12 Families
Acta Haematol (2009) 121 (2-3): 106–110.
This article has been cited by the following articles in journals that are participating in CrossRef Cited-by Linking.
- Anne Goodeve
Hematology (2016) 2016 (1): 678.
Alterations of mRNA processing and stability as a pathogenic mechanism in von Willebrand factor quantitative deficiencies
- G. CASTAMAN
- M. PLATÈ
- S.H. GIACOMELLI
- F. RODEGHIERO
- S. DUGA
Journal of Thrombosis and Haemostasis (2010) 8 (12): 2736.