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...

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Detalles Bibliográficos
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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Article
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

Internet

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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