Načítá se...
Complete absence of Cockayne syndrome group B gene product gives rise to UV-sensitive syndrome but not Cockayne syndrome
UV-sensitive syndrome (UV(s)S) is a rare autosomal recessive disorder characterized by photosensitivity and mild freckling but without neurological abnormalities or skin tumors. UV(s)S cells show UV hypersensitivity and defective transcription-coupled DNA repair of UV damage. It was suggested that U...
Uloženo v:
| Hlavní autoři: | , , , , , , , |
|---|---|
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
National Academy of Sciences
2004
|
| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC524447/ https://ncbi.nlm.nih.gov/pubmed/15486090 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0404587101 |
| Tagy: |
Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!
|