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Copy number variation of the SELENBP1 gene in schizophrenia
BACKGROUND: Schizophrenia is associated with rare copy-number (CN) mutations. Screening for such alleles genome-wide, though comprehensive, cannot study in-depth the causality of particular loci, therefore cannot provide the functional interpretation for the disease etiology. We hypothesized that CN...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2915948/ https://ncbi.nlm.nih.gov/pubmed/20615253 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1744-9081-6-40 |
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