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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...
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| Asıl Yazarlar: | , , , , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
National Academy of Sciences
2004
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| Konular: | |
| Online Erişim: | 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 |
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