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A replication study of schizophrenia-related rare copy number variations in a Han Southern Chinese population
BACKGROUND: Schizophrenia (SCZ) is a common, complex and severe psychiatric disorder associated with many different genetic and environmental risk factors. Evidence from genetic studies has revealed the role of genome structural variations, specifically copy number variants (CNVs), in the etiology o...
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| Publicado no: | Hereditas |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5237532/ https://ncbi.nlm.nih.gov/pubmed/28096781 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s41065-016-0025-x |
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