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Sensitivity to gene dosage and gene expression affects genes with copy number variants observed among neuropsychiatric diseases
BACKGROUND: Copy number variants (CNVs) have been reported to be associated with diseases, traits, and evolution. However, it is hard to determine which gene should have priority as a target for further functional experiments if a CNV is rare or a singleton. In this study, we attempted to overcome t...
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| Vydáno v: | BMC Med Genomics |
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| Hlavní autoři: | , , , , , , , , , , , , , , , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2020
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7104509/ https://ncbi.nlm.nih.gov/pubmed/32223758 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12920-020-0699-9 |
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