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On the traces of XPD: cell cycle matters - untangling the genotype-phenotype relationship of XPD mutations
Mutations in the human gene coding for XPD lead to segmental progeria - the premature appearance of some of the phenotypes normally associated with aging - which may or may not be accompanied by increased cancer incidence. XPD is required for at least three different critical cellular functions: in...
| Autores principales: | , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2010
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2949746/ https://www.ncbi.nlm.nih.gov/pubmed/20840796 http://dx.doi.org/10.1186/1747-1028-5-24 |