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The role of Cockayne Syndrome group B (CSB) protein in base excision repair and aging
Cockayne Syndrome (CS) is a rare human genetic disorder characterized by progressive multisystem degeneration and segmental premature aging. The CS complementation group B (CSB) protein is engaged in transcription coupled and global nucleotide excision repair, base excision repair and general transc...
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| Autores principales: | , , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
2008
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2538557/ https://ncbi.nlm.nih.gov/pubmed/18541289 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.mad.2008.04.009 |
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