Investigation of the involvement of MIR185 and its target genes in the development of schizophrenia

BACKGROUND: Schizophrenia is a complex neuropsychiatric disorder of unclear etiology. The strongest known genetic risk factor is the 22q11.2 microdeletion. Research has yet to confirm which genes within the deletion region are implicated in schizophrenia. The minimal 1.5 megabase deletion contains M...

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Bibliografiset tiedot
Päätekijät: Forstner, Andreas J., Basmanav, F. Buket, Mattheisen, Manuel, Böhmer, Anne C., Hollegaard, Mads V., Janson, Esther, Strengman, Eric, Priebe, Lutz, Degenhardt, Franziska, Hoffmann, Per, Herms, Stefan, Maier, Wolfgang, Mössner, Rainald, Rujescu, Dan, Ophoff, Roel A., Moebus, Susanne, Mortensen, Preben B., Børglum, Anders D., Hougaard, David M., Frank, Josef, Witt, Stephanie H., Rietschel, Marcella, Zimmer, Andreas, Nöthen, Markus M., Miró, Xavier, Cichon, Sven
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Canadian Medical Association 2014
Aiheet:
Research Papers
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC4214873/
https://ncbi.nlm.nih.gov/pubmed/24936775
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1503/jpn.130189
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