Mutational analysis of ERCC3, which is involved in DNA repair and transcription initiation: identification of domains essential for the DNA repair function.

The human ERCC3 gene, which corrects specifically the nucleotide excision repair defect in human xeroderma pigmentosum group B and cross-complements the repair deficiency in rodent UV-sensitive mutants of group 3, encodes a presumed DNA helicase that is identical to the p89 subunit of the general tr...

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Hlavní autoři: Ma, L, Westbroek, A, Jochemsen, A G, Weeda, G, Bosch, A, Bootsma, D, Hoeijmakers, J H, van der Eb, A J
Médium: Artigo
Jazyk:Inglês
Vydáno: 1994
Témata:
Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC358778/
https://ncbi.nlm.nih.gov/pubmed/8196650
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