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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Detaylı Bibliyografya
Yayımlandı:J Endocr Soc
Asıl Yazarlar: Choi, Heewon, Hong, Namki, Shin, Saeam, Lee, Seung Tae, Choi, Jong Rak, Kang, Sang Wook, Rhee, Yumie
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Oxford University Press 2020
Konular:
Adrenal
Online Erişim: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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