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Genetic copy number variants in sib pairs both affected with schizophrenia
BACKGROUND: Schizophrenia is a complex disorder with involvement of multiple genes. METHODS: In this study, genome-wide screening for DNA copy-number variations (CNVs) was conducted for ten pairs, a total of 20 cases, of affected siblings using oligonucleotide array-based CGH. RESULTS: We found nega...
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| Hoofdauteurs: | , , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
BioMed Central
2010
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2843606/ https://ncbi.nlm.nih.gov/pubmed/20064257 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1423-0127-17-2 |
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