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...

Descrizione completa

Dettagli Bibliografici

Pubblicato in:	Nucleic Acids Res
Autori principali:	Koken, M H, Vreeken, C, Bol, S A, Cheng, N C, Jaspers-Dekker, I, Hoeijmakers, J H, Eeken, J C, Weeda, G, Pastink, A
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	Oxford University Press 1992
Accesso online:	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
Tags:	Aggiungi Tag Nessun Tag, puoi essere il primo ad aggiungerne!!