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MON-321 Metastatic Melanoma with Unknown Primary Site in a Patient with Multiple Endocrine Neoplasia Type 1

Background: MEN1 is a rare hereditary tumor syndrome caused by germline inactivating mutations of the tumor suppressor gene MEN1 and is characterized by a predisposition to endocrine tumors primarily of parathyroid, enteropancreatic, and anterior pituitary origin, as well as nonendocrine neoplasms....

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Detalles Bibliográficos
Autores principales:	Kamilaris, Crystal, Mandl, Adel, Simonds, William, Weinstein, Lee, Agarwal, Sunita, Blau, Jenny
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Endocrine Society 2019
Materias:	Tumor Biology
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6550817/ http://dx.doi.org/10.1210/js.2019-MON-321

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