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Somatic RET mutation in a patient with pigmented adrenal pheochromocytoma
Pheochromocytomas (PCC) and paraganglioma (PGL) are rare neuroendocrine tumors arising from chromaffin cells of the neural crest. Mutations in the RET-proto-oncogene are associated with sporadic pheochromocytoma, familial or sporadic medullary thyroid carcinoma (MTC) and multiple endocrine neoplasia...
Autores principales: | Maison, Nicole, Korpershoek, Esther, Eisenhofer, Graeme, Robledo, Mercedes, de Krijger, Ronald, Beuschlein, Felix |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bioscientifica Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4738194/ https://www.ncbi.nlm.nih.gov/pubmed/26843961 http://dx.doi.org/10.1530/EDM-15-0117 |
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