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The VHL gene is epigenetically inactivated in pheochromocytomas and abdominal paragangliomas
Pheochromocytoma (PCC) and abdominal paraganglioma (PGL) are neuroendocrine tumors that present with clinical symptoms related to increased catecholamine levels. About a third of the cases are associated with constitutional mutations in pre-disposing genes, of which some may also be somatically muta...
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| Päätekijät: | , , , , , , , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Landes Bioscience
2013
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3933494/ https://ncbi.nlm.nih.gov/pubmed/24149047 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4161/epi.26686 |
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