Cloning and characterization of the Drosophila homolog of the xeroderma pigmentosum complementation-group B correcting gene, ERCC3.

Previously the human nucleotide excision repair gene ERCC3 was shown to be responsible for a rare combination of the autosomal recessive DNA repair disorders xeroderma pigmentosum (complementation group B) and Cockayne's syndrome (complementation group C). The human and mouse ERCC3 proteins contain...

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Dades bibliogràfiques

Publicat a:	Nucleic Acids Res
Autors principals:	Koken, M H, Vreeken, C, Bol, S A, Cheng, N C, Jaspers-Dekker, I, Hoeijmakers, J H, Eeken, J C, Weeda, G, Pastink, A
Format:	Artigo
Idioma:	Inglês
Publicat:	Oxford University Press 1992
Accés en línia:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC334384/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1454518/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/20.21.5541
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