A neurogenetic model for the study of schizophrenia spectrum disorders: the International 22q11.2 Deletion Syndrome Brain Behavior Consortium

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 gen...

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Vydáno v:Mol Psychiatry
Hlavní autoři: Gur, RE, Bassett, AS, McDonald-McGinn, DM, Bearden, CE, Chow, E, Emanuel, BS, Owen, M, Swillen, A, Van den Bree, M, Vermeesch, J, Vorstman, JAS, Warren, S, Lehner, T, Morrow, B
Médium: Artigo
Jazyk:Inglês
Vydáno: 2017
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Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5935262/
https://ncbi.nlm.nih.gov/pubmed/28761081
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/mp.2017.161
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