Somatic SDHA mutations in paragangliomas in siblings-Reference-Cited by-同舟云学术

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Somatic SDHA mutations in paragangliomas in siblings

Published:2020-10-09 Issue:41 Volume:99 Page:e22497
ISSN:0025-7974
Container-title:Medicine
language:en
Short-container-title:

Author:

Huang Yen-Chun,Chang Hsiao-Huang,Chen Ming-Huang,Huang Kuo-Hung,Li Anna Fen-Yau,Lin Chien-Hsing,Shyr Yi-Ming,Fang Wen-Liang

Funder

Taipei Veterans General Hospital

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

Reference46 articles.

1. Incidence of pheochromocytoma and sympathetic paraganglioma in the Netherlands: a nationwide study and systematic review;Berends;Euro J Intern Med,2018

2. Malignant paraganglioma of the mesentery: a case report and review of literature;Chetrit;World J Surg Oncol,2012

3. Malignant head and neck paragangliomas in SDHB mutation carriers;Boedeker;Otolaryngol Head Neck Surg,2007

4. Paraganglioma and phaeochromocytoma: from genetics to personalized medicine;Favier;Nat Rev Endocrinol,2015

5. Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma;Baysal;Science,2000

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Application value of whole exome sequencing in screening and identifying novel mutations of hypopharyngeal cancer;Scientific Reports;2023-01-03

2. Mitochondrial respiratory complexes: Significance in human mitochondrial disorders and cancers;Journal of Cellular Physiology;2022-09-08

3. Somatic Mutation Profiling in Head and Neck Paragangliomas;The Journal of Clinical Endocrinology & Metabolism;2022-04-23

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