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Inherited platelet diseases with normal platelet count: phenotypes, genotypes and diagnostic strategy
Inherited platelet disorders resulting from platelet function defects and a normal platelet count cause a moderate or severe bleeding diathesis. Since the description of Glanzmann thrombasthenia resulting from defects of ITGA2B and ITGB3, new inherited platelet disorders have been discovered, facili...
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| Publicat a: | Haematologica |
|---|---|
| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Fondazione Ferrata Storti
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7849565/ https://ncbi.nlm.nih.gov/pubmed/33147934 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3324/haematol.2020.248153 |
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