The bases for Cockayne syndrome

Philip C. Hanawalt ()
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Philip C. Hanawalt: Stanford University

Nature, 2000, vol. 405, issue 6785, 415-415

Abstract: Cockayne syndrome is a rare, inherited human disease that can arise from mutations in any one of five genes, involved in different aspects of DNA repair. New results have now led to a model for how all of these different mutations result in the same disease.

Date: 2000
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DOI: 10.1038/35013197

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