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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Dades bibliogràfiques

Publicat a:	Proc Natl Acad Sci U S A
Autors principals:	Nouspikel, Thierry, Lalle, Philippe, Leadon, Steven A., Cooper, Priscilla K., Clarkson, Stuart G.
Format:	Artigo
Idioma:	Inglês
Publicat:	National Academy of Sciences 1997
Matèries:	Biological Sciences
Accés en línia:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC20331/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/9096355/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.94.7.3116
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