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Genome-wide analysis shows increased frequency of CNV deletions in Dutch schizophrenia patients
BACKGROUND: Since 2008 multiple studies have reported on copy number variations (CNVs) in schizophrenia. However, many regions are unique events with minimal overlap between studies. This makes it difficult to gain a comprehensive overview of all CNVs involved in the aetiology of schizophrenia. We p...
Gorde:
| Egile Nagusiak: | , , , , , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
2011
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3137747/ https://ncbi.nlm.nih.gov/pubmed/21489405 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.biopsych.2011.02.015 |
| Etiketak: |
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