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...

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Publicat a:Endocrinol Diabetes Metab Case Rep
Autors principals: Maison, Nicole, Korpershoek, Esther, Eisenhofer, Graeme, Robledo, Mercedes, de Krijger, Ronald, Beuschlein, Felix
Format: Artigo
Idioma:Inglês
Publicat: Bioscientifica Ltd 2016
Matèries:
Unique/Unexpected Symptoms or Presentations of a Disease
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4738194/
https://ncbi.nlm.nih.gov/pubmed/26843961
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1530/EDM-15-0117
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