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 con...

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Hlavní autoři: Koken, M H, Vreeken, C, Bol, S A, Cheng, N C, Jaspers-Dekker, I, Hoeijmakers, J H, Eeken, J C, Weeda, G, Pastink, A
Médium: Artigo
Jazyk:Inglês
Vydáno: 1992
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC334384/
https://ncbi.nlm.nih.gov/pubmed/1454518
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