RET T244I Germline Variant Mutation in a Patient with Pancreatic Paraganglioma and Primary Hyperparathyroidism

INTRODUCTION: Paragangliomas are rare neuroendocrine tumors that arise from chromaffin cells. Often termed extra-adrenal pheochromocytomas, these tumors vary with regards to their functionality, location, and malignant potential. Mutations in the RET proto-oncogene are associated with multiple endoc...

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Detalles Bibliográficos
Autores principales: Kim, Minha, Aploks, Krist, Vargas-Pinto, Susana, Dong, Xiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Brieflands 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9661538/
https://www.ncbi.nlm.nih.gov/pubmed/36407031
http://dx.doi.org/10.5812/ijem-121056

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9661538/
https://www.ncbi.nlm.nih.gov/pubmed/36407031
http://dx.doi.org/10.5812/ijem-121056

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