Correction of xeroderma pigmentosum complementation group D mutant cell phenotypes by chromosome and gene transfer: involvement of the human ERCC2 DNA repair gene.

Cultured cells from individuals afflicted with the genetically heterogeneous autosomal recessive disorder xeroderma pigmentosum (XP) exhibit sensitivity to UV radiation and defective nucleotide excision repair. Complementation of these mutant phenotypes after the introduction of single human chromos...

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Detaylı Bibliyografya
Asıl Yazarlar: Flejter, W L, McDaniel, L D, Johns, D, Friedberg, E C, Schultz, R A
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1992
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC48216/
https://ncbi.nlm.nih.gov/pubmed/1729695
Etiketler: Etiketle
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