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Werner syndrome through the lens of tissue and tumour genomics
Werner syndrome (WS) is the canonical adult human progeroid (‘premature aging’) syndrome. Patients with this autosomal recessive Mendelian disorder display constitutional genomic instability and an elevated risk of important age-associated diseases including cancer. Remarkably few analyses of WS pat...
Autores principales: | Tokita, Mari, Kennedy, Scott R., Risques, Rosa Ana, Chun, Stephen G., Pritchard, Colin, Oshima, Junko, Liu, Yan, Bryant-Greenwood, Peter K., Welcsh, Piri, Monnat, Raymond J. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4997333/ https://www.ncbi.nlm.nih.gov/pubmed/27559010 http://dx.doi.org/10.1038/srep32038 |
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