A rare deletion at distal 16p11.2 is implicated in schizophrenia

CONTEXT: Large genomic copy number variations (CNVs) have been implicated as strong risk factors for schizophrenia. However, the rarity of these events has created challenges for the identification of further pathogenic loci, and extremely large samples are required to provide convincing replication...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Guha, Saurav, Rees, Elliott, Darvasi, Ariel, Ivanov, Dobril, Ikeda, Masashi, Bergen, Sarah E., Magnusson, Patrik K, Cormican, Paul, Morris, Derek, Gill, Michael, Cichon, Sven, Rosenfeld, Jeffrey A., Lee, Annette, Gregersen, Peter K., Kane, John M., Malhotra, Anil K., Rietschel, Marcella, Nöthen, Markus M., Degenhardt, Franziska, Priebe, Lutz, Breuer, René, Strohmaier, Jana, Ruderfer, Douglas M, Moran, Jennifer L, Chambert, Kimberly D, Sanders, Alan R., Shi, Jianxin, Kendler, Kenneth, Riley, Brien, O’Neill, Tony, Walsh, Dermot, Malhotra, Dheeraj, Corvin, Aiden, Purcell, Shaun, Sklar, Pamela, Iwata, Nakao, Hultman, Christina M, Sullivan, Patrick F., Sebat, Jonathan, McCarthy, Shane, Gejman, Pablo V., Levinson, Douglas F., Owen, Michael J, O’Donovan, Michael C, Lencz, Todd, Kirov, George
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 2013
Pynciau:
Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC3750982/
https://ncbi.nlm.nih.gov/pubmed/23325106
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1001/2013.jamapsychiatry.71
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