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Inherited mutations in pheochromocytoma and paraganglioma: why all patients should be offered genetic testing
BACKGROUND: Pheochromocytomas (PCC) and paragangliomas (PGL) are neuroendocrine tumors which, although rare, are an important cause of secondary hypertension because of the high morbidity and mortality. PCC/PGL are still thought of as the “tumor of tens” with 10% being hereditary; however, recent po...
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| Pubblicato in: | Ann Surg Oncol |
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| Autori principali: | , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2013
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4291281/ https://ncbi.nlm.nih.gov/pubmed/23512077 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1245/s10434-013-2942-5 |
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