A common mutational pattern in Cockayne syndrome patients from xeroderma pigmentosum group G: Implications for a second XPG function

Xeroderma pigmentosum (XP) patients have defects in nucleotide excision repair (NER), the versatile repair pathway that removes UV-induced damage and other bulky DNA adducts. Patients with Cockayne syndrome (CS), another rare sun-sensitive disorder, are specifically defective in the preferential rem...

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Bibliografiska uppgifter
Huvudupphovsmän: Nouspikel, Thierry, Lalle, Philippe, Leadon, Steven A., Cooper, Priscilla K., Clarkson, Stuart G.
Materialtyp: Artigo
Språk:Inglês
Publicerad: The National Academy of Sciences of the USA 1997
Ämnen:
Biological Sciences
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC20331/
https://ncbi.nlm.nih.gov/pubmed/9096355
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