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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Detalles Bibliográficos
Autores principales: Amar, Shirly, Ovadia, Ofer, Maier, Wolfgang, Ebstein, Richard, Belmaker, RH, Mishmar, Dan, Agam, Galila
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2915948/
https://www.ncbi.nlm.nih.gov/pubmed/20615253
http://dx.doi.org/10.1186/1744-9081-6-40

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2915948/
https://www.ncbi.nlm.nih.gov/pubmed/20615253
http://dx.doi.org/10.1186/1744-9081-6-40

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