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An interaction-based model for neuropsychiatric features of copy-number variants
Variably expressive copy-number variants (CNVs) are characterized by extensive phenotypic heterogeneity of neuropsychiatric phenotypes. Approaches to identify single causative genes for these phenotypes within each CNV have not been successful. Here, we posit using multiple lines of evidence, includ...
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| Vydáno v: | PLoS Genet |
|---|---|
| Hlavní autoři: | , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Public Library of Science
2019
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6336245/ https://ncbi.nlm.nih.gov/pubmed/30653500 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1007879 |
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