MON-195 Genetic Analysis and Clinical Characteristics of Hereditary Paraganglioma and Pheochromocytoma Syndrome in Korean Population

Pheochromocytoma (PCC) and paragangliomas (PGL), rare neuroendocrine tumor originating from the chromaffin cells together referred as PPGL, are acknowledged to be more than 40% hereditary, related to germline mutations of susceptibility gene. With the advancement of genetic analysis technique, inclu...

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Detalles Bibliográficos
Publicado en:J Endocr Soc
Autores principales: Choi, Heewon, Hong, Namki, Shin, Saeam, Lee, Seung Tae, Choi, Jong Rak, Kang, Sang Wook, Rhee, Yumie
Formato: Artigo
Lenguaje:Inglês
Publicado: Oxford University Press 2020
Materias:
Adrenal
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC7209484/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jendso/bvaa046.879
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