Penetrance of phaeochromocytoma in RET G533C carriers differs between South America and Europe
Author:
Publisher
Bioscientifica
Subject
Cancer Research,Endocrinology,Oncology,Endocrinology, Diabetes and Metabolism
Reference26 articles.
1. A rare RET gene exon 8 mutation is found in two Greek kindreds with familial medullary thyroid carcinoma implications for screening;Clinical Endocrinology,2006
2. The penetrance of men pheochromocytoma is not only determined by ret mutations - Related https org;Endocrine Cancer,2017
3. Multiple endocrine neoplasia type 2A due to an exon 8 (G533C) mutation in a large North American kindred;Thyroid,2013
4. First reported case in Ireland of MEN2A due to a rare mutation in exon 8 of the RET oncogene;Endocrinolology Diabetes and Metabolism Case Reports,2013
5. The RET p.G533C mutation confers predisposition to multiple endocrine neoplasia type 2A in a Brazilian kindred and is able to induce a malignant phenotype in vitro and in vivo;Thyroid,2011
Cited by 2 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. Multiple endocrine neoplasia type 2: A review;Seminars in Cancer Biology;2021-04
2. Genotype and phenotype landscape of MEN2 in 554 medullary thyroid cancer patients: the BrasMEN study;Endocrine Connections;2019-03
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