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

BACKGROUND: Pheochromocytoma and paragangliomas (PPGL) are hereditary in approximately 30% to 40% cases. With the advancement of genetic analysis techniques, including next-generation sequencing (NGS), there were attempts to classify PPGL into molecular clusters. With NGS being applied to clinical s...

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Detalles Bibliográficos
Autores principales: Choi, Heewon, Kim, Kyoung Jin, Hong, Namki, Shin, Saeam, Choi, Jong-Rak, Kang, Sang Wook, Lee, Seung Tae, Rhee, Yumie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Endocrine Society 2020
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7803615/
https://www.ncbi.nlm.nih.gov/pubmed/33397040
http://dx.doi.org/10.3803/EnM.2020.683

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7803615/
https://www.ncbi.nlm.nih.gov/pubmed/33397040
http://dx.doi.org/10.3803/EnM.2020.683

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