Germline copy number variations are associated with breast cancer risk and prognosis

Breast cancer is one of the most common cancers among women, and susceptibility is explained by genetic, lifestyle and environmental components. Copy Number Variants (CNVs) are structural DNA variations that contribute to diverse phenotypes via gene-dosage effects or cis-regulation. In this study, w...

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Detalles Bibliográficos
Autores principales: Kumaran, Mahalakshmi, Cass, Carol E., Graham, Kathryn, Mackey, John R., Hubaux, Roland, Lam, Wan, Yasui, Yutaka, Damaraju, Sambasivarao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5677082/
https://www.ncbi.nlm.nih.gov/pubmed/29116104
http://dx.doi.org/10.1038/s41598-017-14799-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5677082/
https://www.ncbi.nlm.nih.gov/pubmed/29116104
http://dx.doi.org/10.1038/s41598-017-14799-7

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