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...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Endocrinol Diabetes Metab Case Rep
Main Authors: Maison, Nicole, Korpershoek, Esther, Eisenhofer, Graeme, Robledo, Mercedes, de Krijger, Ronald, Beuschlein, Felix
Formato: Artigo
Idioma:Inglês
Publicado em: Bioscientifica Ltd 2016
Assuntos:
Unique/Unexpected Symptoms or Presentations of a Disease
Acesso em linha: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
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados