Germline SDHB and SDHD mutations in pheochromocytoma and paraganglioma patients

Pheochromocytoma and paragangliomas (PCC/PGL) are neuroendocrine tumors that arise from chromaffin cells of the adrenal medulla and sympathetic/parasympathetic ganglia, respectively. Of clinical relevance regarding diagnosis is the highly variable presentation of symptoms in PCC/PGL patients. To dat...

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Bibliographic Details
Published in:Endocr Connect
Main Authors: Huang, Yiqiang, Wang, Lin-ang, Xie, Qiubo, Pang, Jian, Wang, Luofu, Yi, Yuting, Zhang, Jun, Zhang, Yao, Chen, Rongrong, Lan, Weihua, Zhang, Dianzheng, Jiang, Jun
Format: Artigo
Language:Inglês
Published: Bioscientifica Ltd 2018
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Research
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC6240141/
https://ncbi.nlm.nih.gov/pubmed/30352407
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1530/EC-18-0325
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