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CSF3R T618I is a highly prevalent and specific mutation in chronic neutrophilic leukemia
Truncation mutations of the receptor cytoplasmic domain for colony-stimulating factor 3 (CSF3R) are frequently seen in severe congenital neutropenia, whereas activating missense mutations affecting the extracellular domain (exon 14) have been described in hereditary neutrophilia and chronic neutroph...
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| Main Authors: | , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4100617/ https://ncbi.nlm.nih.gov/pubmed/23604229 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/leu.2013.122 |
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