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Article

A novel mutation of the WRN gene in a Chinese patient with Werner syndrome.

Clinical and experimental dermatology - 1 May 2008

Zhao N, Hao F, Qu T, Zuo Y-G, Wang B-X

Abstract excerpt

Werner syndrome (WS) is an autosomal recessive inherited disease characterized by features of premature ageing. It is caused by mutations of the WRN gene encoding a protein with both exonuclease and helicase activities. The aim of this study was to identify gene mutations in a Chinese patient with WS. A 31-year-old Chinese man with typical features of WS was diagnosed as having probable WS. We performed PCR to...

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Source

Identifiers

PMID: 18205852
DOI: 10.1111/j.1365-2230.2007.02641.x

Genes

WRN

Provenance

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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