Structure and expression of the human XPBC/ERCC-3 gene involved in DNA repair disorders xeroderma pigmentosum and Cockayne's syndrome.

The human XPBC/ERCC-3 was cloned by virtue of its ability to correct the excision repair defect of UV-sensitive rodent mutants of complementation group 3. The gene appeared to be in addition implicated in the human, cancer prone repair disorder xeroderma pigmentosum group B, which is also associated...

Szczegółowa specyfikacja

Opis bibliograficzny

Wydane w:	Nucleic Acids Res
Główni autorzy:	Weeda, G, Ma, L B, van Ham, R C, van der Eb, A J, Hoeijmakers, J H
Format:	Artigo
Język:	Inglês
Wydane:	Oxford University Press 1991
Dostęp online:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC329143/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1956789/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/19.22.6301
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