Visual processing deficits in 22q11.2 Deletion Syndrome

Carriers of the rare 22q11.2 microdeletion present with a high percentage of positive and negative symptoms and a high genetic risk for schizophrenia. Visual processing impairments have been characterized in schizophrenia, but less so in 22q11.2 Deletion Syndrome (DS). Here, we focus on visual proce...

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Detaylı Bibliyografya
Yayımlandı:Neuroimage Clin
Asıl Yazarlar: Biria, Marjan, Tomescu, Miralena I., Custo, Anna, Cantonas, Lucia M., Song, Kun-Wei, Schneider, Maude, Murray, Micah M., Eliez, Stephan, Michel, Christoph M., Rihs, Tonia A.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Elsevier 2017
Konular:
Regular Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5842759/
https://ncbi.nlm.nih.gov/pubmed/29527499
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nicl.2017.12.028
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