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Article

Genetic analysis of a Chinese Han family with multiple endocrine neoplasia type 2A.

Indian journal of biochemistry & biophysics - 1 Feb 2013

Guo Yi, Xu Hongbo, Ren Zuhai, Yang Yongjia, Xiong Wei, Gao Kai, Li Xiaorong, Luo Ziqiang, Deng Hao

Abstract excerpt

Multiple endocrine neoplasia type 2 (MEN2) is an autosomal dominant disorder that can be distinguished as three different syndromes: multiple endocrine neoplasia type 2A (MEN2A), MEN2B and familial medullary thyroid carcinoma (FMTC). This disorder is usually caused by the mutations of the rearranged during transfection protooncogene gene (RET) or the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1). To...

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Identifiers

PMID: 23617071

Genes

RET
NTRK1

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Genetic analysis of a Chinese Han family with multiple endocrine neoplasia type 2A.PMID 23617071Read ↗

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[A comparison of clinical characteristics between 2 pedigrees of multiple endocrine neoplasia type 2A with different RET mutations].Semantic proximity Read ↗

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RET proto-oncogene mutations are restricted to codons 634 and 918 in mainland Chinese families with MEN2A and MEN2B.Semantic proximity Read ↗

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