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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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Detaylı Bibliyografya
Yayımlandı:Nature
Asıl Yazarlar: BOUMA, B. N., HORDIJK-HOS, J. M., DE GRAAF, S., SIXMA, J. J., VAN MOURIK, J. A.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Nature Publishing Group UK 1975
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC7086501/
https://ncbi.nlm.nih.gov/pubmed/1080838
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/257510a0
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