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Article

Mutation analysis in a Chinese family with multiple endocrine neoplasia type 1.

Chinese medical journal - 5 Mar 2010

Zha Bing-bing, Liang Wang, Liu Jun, Cheng Juan, Hong Xiao-wu, Liu Jing, Li Yi-ming, Ma Duan

Abstract excerpt

BACKGROUND: Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant cancer syndrome which is caused by germline mutations of the tumor suppressor gene MEN1. This study aimed to identify mutations in a Chinese pedigree with MEN1. METHODS: A large Chinese family with MEN1 was collected. All of the coded regions and their adjacent sequences of the MEN1 gene were amplified and sequenced. RESULTS: In this...

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Share to MEN1 gene
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Polymorphism, Single Nucleotide

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Share to Sequence Analysis, DNA

Source

Identifiers

PMID: 20367983

Genes

MEN1

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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