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...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Endocrinol Metab (Seoul)
Prif Awduron: 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
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Korean Endocrine Society 2020
Pynciau:
Original Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC7803589/
https://ncbi.nlm.nih.gov/pubmed/33397043
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3803/EnM.2020.756
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