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Article

A C. elegans homolog of the Cockayne syndrome complementation group A gene.

DNA repair - 1 Dec 2014

Babu Vipin, Hofmann Kay, Schumacher Björn

Abstract excerpt

Cockayne syndrome (CS) is a debilitating and complex disorder that results from inherited mutations in the CS complementation genes A and B, CSA and CSB. The links between the molecular functions of the CS genes and the complex pathophysiology of CS are as of yet poorly understood and are the subject of intense debate. While mouse models reflect the complexity of CS, studies on simpler genetic models might shed...

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Identifiers

PMID: 25453470
DOI: 10.1016/j.dnarep.2014.09.011
PMCID: PMC4255241

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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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