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Acute promyelocytic leukemia harbouring rare FLT3-TKD and WT1 mutations: A case report
The involvement of the central nervous system (CNS) is rare in acute promyelocytic leukemia (APL). The present study reported the case of a 34-year-old male patient with APL that possessed a rare point mutation (p.Asn841Gly, c.2523C>A) in the tyrosine kinase domain of the FMS-like tyrosine kinase...
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| Pubblicato in: | Oncol Lett |
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| Autori principali: | , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
D.A. Spandidos
2015
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4533715/ https://ncbi.nlm.nih.gov/pubmed/26622765 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/ol.2015.3437 |
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