The bases for Cockayne syndrome

被引：0
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作者：
Philip C. Hanawalt
机构：
[1] Stanford University,Department of Biological Sciences
来源：
Nature | 2000年 / 405卷
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摘要：
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.
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页码：415 / 415
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