Whole Exome Sequencing Identifies Novel Genetic Alterations in Patients with Pheochromocytoma/Paraganglioma

BACKGROUND: Pheochromocytoma and paragangliomas (PPGL) are known as tumors with the highest level of heritability, approximately 30% of all cases. Clinical practice guidelines of PPGL recommend genetic testing for germline variants in all patients. In this study, we used whole exome sequencing to id...

Descripción completa

Detalles Bibliográficos
Autores principales: Seo, Soo Hyun, Kim, Jung Hee, Kim, Man Jin, Cho, Sung Im, Kim, Su Jin, Kang, Hyein, Shin, Chan Soo, Park, Sung Sup, Lee, Kyu Eun, Seong, Moon-Woo
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/PMC7803589/
https://www.ncbi.nlm.nih.gov/pubmed/33397043
http://dx.doi.org/10.3803/EnM.2020.756

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7803589/
https://www.ncbi.nlm.nih.gov/pubmed/33397043
http://dx.doi.org/10.3803/EnM.2020.756

Ejemplares similares