טוען...
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...
שמור ב:
| הוצא לאור ב: | Genet Res (Camb) |
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| Main Authors: | , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Cambridge University Press
2014
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| נושאים: | |
| גישה מקוונת: | 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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