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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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| Опубликовано в: : | Nature |
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| Главные авторы: | , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Nature Publishing Group UK
1975
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| Предметы: | |
| Online-ссылка: | 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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