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Characterization of single gene copy number variants in schizophrenia
BACKGROUND: Genetic studies of schizophrenia have implicated numerous risk loci including several copy number variants (CNVs) of large effect and hundreds of loci of small effect. In only a few cases has a specific gene been clearly identified. Rare CNVs affecting a single gene offer a potential ave...
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| Vydáno v: | Biol Psychiatry |
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| Hlavní autoři: | , , , , , , , , , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2019
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7103483/ https://ncbi.nlm.nih.gov/pubmed/31767120 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.biopsych.2019.09.023 |
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