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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...
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 |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2015
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Materias: | |
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 |
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