Copy number variation associates with mortality in long‐lived individuals: a genome‐wide assessment

Copy number variants (CNVs) represent a significant source of genetic variation in the human genome and have been implicated in numerous diseases and complex traits. To date, only a few studies have investigated the role of CNVs in human lifespan. To investigate the impact of CNVs on prospective mor...

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Detalles Bibliográficos
Autores principales: Nygaard, Marianne, Debrabant, Birgit, Tan, Qihua, Deelen, Joris, Andersen‐Ranberg, Karen, de Craen, Anton J.M., Beekman, Marian, Jeune, Bernard, Slagboom, Pieternella E., Christensen, Kaare, Christiansen, Lene
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4717275/
https://www.ncbi.nlm.nih.gov/pubmed/26446717
http://dx.doi.org/10.1111/acel.12407

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4717275/
https://www.ncbi.nlm.nih.gov/pubmed/26446717
http://dx.doi.org/10.1111/acel.12407

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