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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Detaylı Bibliyografya
Asıl Yazarlar: 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
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Canadian Medical Association 2014
Konular:
Research Papers
Online Erişim: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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