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Common alleles contribute to schizophrenia in CNV carriers
The genetic architecture of schizophrenia is complex, involving risk alleles ranging from common alleles of weak effect to rare alleles of large effect, the best exemplar of the latter being large copy number variants (CNVs). It is currently unknown whether pathophysiology in those with defined rare...
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| Vydáno v: | Mol Psychiatry |
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| Hlavní autoři: | , , , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Nature Publishing Group
2016
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4960448/ https://ncbi.nlm.nih.gov/pubmed/26390827 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/mp.2015.143 |
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