Identification of rare variants in KCTD13 at the schizophrenia risk locus 16p11.2

Duplications in 16p11.2 are a risk factor for schizophrenia (SCZ). Using genetically modified zebrafish, Golzio and colleagues identified KCTD13 within 16p11.2 as a major driver of the neuropsychiatric phenotype observed in humans. The aims of the present study were to explore the role of KCTD13 in...

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Veröffentlicht in:Psychiatr Genet
Hauptverfasser: Degenhardt, Franziska, Heinemann, Barbara, Strohmaier, Jana, Pfohl, Marvin A., Giegling, Ina, Hofmann, Andrea, Ludwig, Kerstin U., Witt, Stephanie H., Ludwig, Michael, Forstner, Andreas J., Albus, Margot, Schwab, Sibylle G., Borrmann-Hassenbach, Margitta, Lennertz, Leonard, Wagner, Michael, Hoffmann, Per, Rujescu, Dan, Maier, Wolfgang, Cichon, Sven, Rietschel, Marcella, Nöthen, Markus M.
Format: Artigo
Sprache:Inglês
Veröffentlicht: Lippincott Williams & Wilkins 2016
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Brief Reports
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5087564/
https://ncbi.nlm.nih.gov/pubmed/27668412
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/YPG.0000000000000145
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