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Translational Diagnostics and Therapeutics in Pancreatic Neuroendocrine Tumors
Pancreatic neuroendocrine tumors (PNETs) are rare tumors, but have been increasing in incidence. Although typically thought of as indolent, more than half of patients present with metastatic disease. For many years, the only mutations commonly known in these tumors were those in the MEN1 gene. Recen...
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| Publicado no: | Clin Cancer Res |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5082425/ https://ncbi.nlm.nih.gov/pubmed/27742788 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1158/1078-0432.CCR-16-0435 |
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