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Impact of copy number variations burden on coding genome in humans using integrated high resolution arrays
Copy number variations (CNVs) alter the transcriptional and translational levels of genes by disrupting the coding structure and this burden of CNVs seems to be a significant contributor to phenotypic variations. Therefore it was necessary to assess the complexities of CNV burden on the coding genom...
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| Publicado no: | Genet Res (Camb) |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Cambridge University Press
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7045015/ https://ncbi.nlm.nih.gov/pubmed/25578402 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1017/S0016672314000202 |
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