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RET c.1901G>A and Novel SLC12A3 Mutations in Familial Pheochromocytomas

Genes - 12 May 2022

Zhao Lin, Yang Kun-Qi, Fan Peng, Gong Ding-Xu, Zhang Lin, Lu Yi-Ting, Meng Xu, Zhou Xian-Liang

Abstract excerpt

Familial PHEOs (pheochromocytomas) are inherited as an autosomal dominant trait, and inherited PHEOs can be one clinical phenotype of clinical syndromes, such as multiple endocrine neoplasia type 2A (MEN2A). In recent years, there has been a lot of controversy about the factors affecting the penetrance of PHEOs in MEN2A, of which the effects of RET (rearranged during transfection) proto-oncogene mutations are the...

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PMID: 35627249
DOI: 10.3390/genes13050864
PMCID: PMC9140906

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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