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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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Bibliografske podrobnosti
izdano v:Nature
Main Authors: BOUMA, B. N., HORDIJK-HOS, J. M., DE GRAAF, S., SIXMA, J. J., VAN MOURIK, J. A.
Format: Artigo
Jezik:Inglês
Izdano: Nature Publishing Group UK 1975
Teme:
Online dostop: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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