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...

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Dades bibliogràfiques

Publicat a:	Nucleic Acids Res
Autors principals:	Weeda, G, Ma, L B, van Ham, R C, van der Eb, A J, Hoeijmakers, J H
Format:	Artigo
Idioma:	Inglês
Publicat:	Oxford University Press 1991
Accés en línia:	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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