Factor H interferes with the adhesion of sickle red cells to vascular endothelium: a novel disease-modulating molecule
Sickle cell disease is an autosomal recessive genetic red cell disorder with a worldwide distribution. Growing evidence suggests a possible involvement of complement activation in the severity of clinical complications of sickle cell disease. In this study we found activation of the alternative comp...
Kaydedildi:
| Asıl Yazarlar: | , , , , , , , , , , , , , , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Ferrata Storti Foundation
2019-05-01
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| Seri Bilgileri: | Haematologica |
| Online Erişim: | https://haematologica.org/article/view/8894 |
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