von Willebrand disease with G4022A mutation (vWd Sungnam): a case report.

A 10-year-old male patient affected by type 2 von Willebrand disease (vWD) and his family members were investigated by hemostatic and molecular genetic studies. The propositus, who experienced frequent bleeding episodes, was characterized by a normal level of von Willebrand factor (vWF) antigen (54%...

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Detalles Bibliográficos
Autores principales: Song, K. S., Kang, S. H., Kang, M. S., Park, Y. S., Choi, J. R., Kim, H. K., Park, Q.
Formato: Texto
Lenguaje:English
Publicado: Korean Academy of Medical Sciences 1999
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3054163/
https://www.ncbi.nlm.nih.gov/pubmed/10102532

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