Schizophrenia: genome, interrupted
- PMID: 18439401
- DOI: 10.1016/j.neuron.2008.04.007
Schizophrenia: genome, interrupted
Abstract
Structural chromosomal variation is increasingly recognized as an important contributor to human diseases, particularly those of neurodevelopment, such as autism. A current paper makes a significant advance to schizophrenia genetics by establishing an association with rare copy number variants (CNV), which are over-represented in neurodevelopmental genes.