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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.
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Journal of Thrombosis and Haemostasis (2010) 8 (12): 2736.