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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Dades bibliogràfiques
Publicat a:J Endocr Soc
Autors principals: Choi, Heewon, Hong, Namki, Shin, Saeam, Lee, Seung Tae, Choi, Jong Rak, Kang, Sang Wook, Rhee, Yumie
Format: Artigo
Idioma:Inglês
Publicat: Oxford University Press 2020
Matèries:
Adrenal
Accés en línia: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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