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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Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς: 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
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: Canadian Medical Association 2014
Θέματα:
Research Papers
Διαθέσιμο Online: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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