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Lack of SF3B1 R625 mutations in cutaneous melanoma
BACKGROUND: Melanoma is a deadly disease affecting people worldwide. Genetic studies have identified different melanoma subtypes characterized by specific recurrently mutated genes and led to the successful clinical introduction of targeted therapies. Hotspot mutations in SF3B1 were recently reporte...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3671181/ https://ncbi.nlm.nih.gov/pubmed/23694694 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1746-1596-8-87 |
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