| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 8814166 | Biological Psychiatry | 2018 | 294 Pages | 
Abstract
												Overall, this study provides biological evidence that the SZ-risk gene DGCR2 regulates critical steps of early corticogenesis possibly through a Reelin-dependent mechanism. Additionally, we found that the SZ-risk mutation in DGCR2 has a pathogenic impact on cortical formation by reducing protein expression level, suggesting a functional role for DGCR2 haploinsufficiency in the 22q11.2 deletion syndrome.
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											Authors
												Aude Molinard-Chenu, Alexandre Dayer, 
											