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Clinical significance of disease‐specific MYD88 mutations in circulating DNA in primary central nervous system lymphoma
Recent sequencing studies demonstrated the MYD88 L265P mutation in more than 70% of primary central nervous system lymphomas (PCNSL), and the clinical significance of this mutation has been proposed as diagnostic and prognostic markers in PCNSL. In contrast, mutational analyses using cell‐free DNAs...
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| Publicado no: | Cancer Sci |
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| Main Authors: | , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5765295/ https://ncbi.nlm.nih.gov/pubmed/29151258 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/cas.13450 |
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