SUN-916 Novel Germline p.Gly42Arg MEN1 Missense Mutation in a Family Harboring Very Aggressive Pancreatic Tumor, Hyperparathyroidism and Pituitary Tumor

Background.Pancreatic neuroendocrine tumors ocurs in 30-80% of patients with MEN-1, and may be non-functioning and hormone secreting tumors. Non-functioning GEP-NETs are increasingly recognised due to advanced imaging modalities such as endoscopic ultrasound thus became the most common type in MEN1...

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Detalles Bibliográficos
Autores principales: Naves, Luciana Ansaneli, Santana, Lidiana B, Miranda, Isabella Santiago M, Rosa, Isabella Naves, Mesquita, Pedro G, Santa Rita, Ticiane H, Sousa, Claudia F, Barra, Gustavo Barcelos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Tumor Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7208008/
http://dx.doi.org/10.1210/jendso/bvaa046.1347

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7208008/
http://dx.doi.org/10.1210/jendso/bvaa046.1347

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