Rare chromosomal deletions and duplications increase risk of schizophrenia
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/nature07239.pdf
Reference32 articles.
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3. Kirov, G. et al. Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia. Hum. Mol. Genet. 17, 458–465 (2008)
4. Flomen, R. H. et al. Association study of CHRFAM7A copy number and 2 bp deletion polymorphisms with schizophrenia and bipolar affective disorder. Am. J. Med. Genet. B. Neuropsychiatr. Genet. 141, 571–575 (2006)
5. Friedman, J. I. et al. CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy. Mol. Psychiatry 13, 261–266 (2008)
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