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Independent estimation of the frequency of rare CNVs in the UK population confirms their role in schizophrenia
BACKGROUND: Several large, rare chromosomal copy number variants (CNVs) have recently been shown to increase risk for schizophrenia and other neuropsychiatric disorders including autism, ADHD, learning difficulties and epilepsy. AIMS: We wanted to examine the frequencies of these schizophrenia-assoc...
| Autores principales: | , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Elsevier
2012
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3315675/ https://www.ncbi.nlm.nih.gov/pubmed/22130109 http://dx.doi.org/10.1016/j.schres.2011.11.004 |