Učitavanje...
A C. elegans homolog of the Cockayne syndrome complementation group A gene
Cockayne syndrome (CS) is a debilitating and complex disorder that result from inherited mutations in the CS complementation genes A and B, CSA and CSB. The links between the molecular functions of the CS genes and the complex pathophysiology of CS are as of yet poorly understood and are the subject...
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| Izdano u: | DNA Repair (Amst) |
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| Glavni autori: | , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2014
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4255241/ https://ncbi.nlm.nih.gov/pubmed/25453470 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.dnarep.2014.09.011 |
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