Germline SDHB and SDHD mutations in pheochromocytoma and paraganglioma patients

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
Main Authors: Yiqiang Huang, Lin-ang Wang, Qiubo Xie, Jian Pang, Luofu Wang, Yuting Yi, Jun Zhang, Yao Zhang, Rongrong Chen, Weihua Lan, Dianzheng Zhang, Jun Jiang
Format: Article
Language:English
Published: Bioscientifica 2018-11-01
Series:Endocrine Connections
Subjects:
PCC/PGL
SDHB
SDHD
genotype–phenotype correlation
Online Access:https://ec.bioscientifica.com/view/journals/ec/7/12/EC-18-0325.xml

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https://ec.bioscientifica.com/view/journals/ec/7/12/EC-18-0325.xml

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