Presence of factor VIII-related antigen in blood platelets of patients with Von Willebrand's disease

VON WILLEBRAND'S disease (VWD) is an autosomally inherited disorder characterised by low factor VIII activity (antihaemophilic factor, AHF), prolonged bleeding time, reduced retention of platelets in a glass bead column and abnormal distocetin-induced platelet aggregation. The prolonged bleedin...

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Detalles Bibliográficos
Autores principales: BOUMA, B. N., HORDIJK-HOS, J. M., DE GRAAF, S., SIXMA, J. J., VAN MOURIK, J. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 1975
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7086501/
https://www.ncbi.nlm.nih.gov/pubmed/1080838
http://dx.doi.org/10.1038/257510a0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7086501/
https://www.ncbi.nlm.nih.gov/pubmed/1080838
http://dx.doi.org/10.1038/257510a0

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