CKN1 (MIM 216400): mutations in Cockayne syndrome type A and a new common polymorphism
Open Access
- 6 December 2003
- journal article
- research article
- Published by Springer Nature in Journal of Human Genetics
- Vol. 49 (1) , 61-63
- https://doi.org/10.1007/s10038-003-0107-2
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
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- Mechanisms of transcription-coupled DNA repairNature Reviews Molecular Cell Biology, 2002
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- A summary of mutations in the UV-sensitive disorders: Xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophyHuman Mutation, 1999
- The Cockayne syndrome group A gene encodes a WD repeat protein that interacts with CSB protein and a subunit of RNA polymerase II TFIIHCell, 1995
- Cockayne syndrome: Review of 140 casesAmerican Journal of Medical Genetics, 1992