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Copy Number Variations in Schizophrenia: Critical Review and New Perspectives on Concepts of Genetics and Disease
OBJECTIVE: Structural variations of DNA, such as copy number variations (CNVs), are recognized to contribute both to normal genomic variability and to risk for human diseases. For example, schizophrenia has an established connection with 22q11.2 deletions. Recent genome-wide studies have provided in...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3295834/ https://ncbi.nlm.nih.gov/pubmed/20439386 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1176/appi.ajp.2009.09071016 |
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