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Hematopoietic transcription factor mutations and inherited platelet dysfunction
The molecular and genetic mechanisms in most patients with inherited platelet dysfunction are unknown. There is increasing evidence that mutations in hematopoietic transcription factors are major players in the pathogenesis of defective megakaryopoiesis and platelet dysfunction in patients with inhe...
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| Publicado no: | F1000Prime Rep |
|---|---|
| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Faculty of 1000 Ltd
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4447035/ https://ncbi.nlm.nih.gov/pubmed/26097739 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12703/P7-66 |
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