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Molecular genetic studies of pancreatic neuroendocrine tumors reveal new therapeutic approaches
Pancreatic neuroendocrine tumors (PNETs) can arise sporadically or as part of familial syndromes. Genetic studies of hereditary syndromes and whole exome sequencing analysis of sporadic PNETs have revealed the roles of some genes involved in PNET tumorigenesis. The most commonly mutated gene in PNET...
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| Yayımlandı: | Endocrinol Metab Clin North Am |
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| Asıl Yazarlar: | , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
2018
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7614857/ https://ncbi.nlm.nih.gov/pubmed/30098714 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ecl.2018.04.007 |
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