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A unified model for the molecular basis of Xeroderma pigmentosum-Cockayne Syndrome
Nucleotide Excision Repair (NER) is a pathway that removes lesions distorting the DNA helix. The molecular basis of the rare diseases Xeroderma pigmentosum (XP) and Cockayne Syndrome (CS) are explained based on the defects happening in 2 NER branches: Global-Genome Repair and Transcription-Coupled R...
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| Publicado no: | Rare Dis |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Taylor & Francis
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4588225/ https://ncbi.nlm.nih.gov/pubmed/26460500 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/21675511.2015.1079362 |
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