Knockdown of the schizophrenia susceptibility gene TCF4 alters gene expression and proliferation of progenitor cells from the developing human neocortex

Background Common variants in the TCF4 gene are among the most robustly supported genetic risk factors for schizophrenia. Rare TCF4 deletions and loss-of-function point mutations cause Pitt–Hopkins syndrome, a developmental disorder associated with severe intellectual disability. Methods To explore...

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Veröffentlicht in:Journal of psychiatry & neuroscience 2017-05, Vol.42 (3), p.181-188
Hauptverfasser: Hill, Matthew J., PhD, Killick, Richard, PhD, Maruszak, Aleksandra, PhD, McLaughlin, Gemma M., MSc, Williams, Brenda P., PhD, Navarrete, Katherinne, PhD, Bray, Nicholas J., PhD
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