A neurogenetic model for the study of schizophrenia spectrum disorders: the International 22q11.2 De...
A neurogenetic model for the study of schizophrenia spectrum disorders: the International 22q11.2 Deletion Syndrome Brain Behavior Consortium
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London: Nature Publishing Group UK
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English
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London: Nature Publishing Group UK
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Contents
Rare copy number variants contribute significantly to the risk for schizophrenia, with the 22q11.2 locus consistently implicated. Individuals with the 22q11.2 deletion syndrome (22q11DS) have an estimated 25-fold increased risk for schizophrenia spectrum disorders, compared to individuals in the general population. The International 22q11DS Brain B...
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A neurogenetic model for the study of schizophrenia spectrum disorders: the International 22q11.2 Deletion Syndrome Brain Behavior Consortium
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TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5935262
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5935262
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ISSN
1359-4184,1476-5578
E-ISSN
1476-5578
DOI
10.1038/mp.2017.161
