Correction of xeroderma pigmentosum repair defect by basal transcription factor BTF2 (TFIIH).

ERCC3 was initially identified as a gene correcting the nucleotide excision repair (NER) defect of xeroderma pigmentosum complementation group B (XP-B). The recent finding that its gene product is identical to the p89 subunit of basal transcription factor BTF2(TFIIH), opened the possibility that it...

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Publicado en:	EMBO J
Autores principales:	van Vuuren, A J, Vermeulen, W, Ma, L, Weeda, G, Appeldoorn, E, Jaspers, N G, van der Eb, A J, Bootsma, D, Hoeijmakers, J H, Humbert, S
Formato:	Artigo
Lenguaje:	Inglês
Publicado:	Nature Publishing Group 1994
Materias:	Research Article
Acceso en línea:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC394995/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8157004/ https://ncbi.nlm.nih.govhttps://doi.org/10.1002/j.1460-2075.1994.tb06428.x
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