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How might stress contribute to increased risk for schizophrenia in children with chromosome 22q11.2 deletion syndrome?
The most common human microdeletion occurs at chromosome 22q11.2. The associated syndrome (22q11.2DS) has a complex and variable phenotype with a high risk of schizophrenia. While the role of stress in the etiopathology of schizophrenia has been under investigation for over 30 years (Walker et al. 2...
| Autores principales: | , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
Springer US
2010
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3056992/ https://www.ncbi.nlm.nih.gov/pubmed/21475728 http://dx.doi.org/10.1007/s11689-010-9069-9 |