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Specific Differences in Temporal Binding Aspects of the Attentional Blink in Chromosome 22q11.2 Deletion Syndrome
Chromosome 22q11.2 Deletion Syndrome (22q11DS) is a genetic syndrome characterized by a variety of cognitive impairments, including difficulty with attention. 22q11DS is the strongest known genetic risk factor for developing schizophrenia, a disorder characterized by impairments in visual attention...
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| Publicado no: | Cortex |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7730721/ https://ncbi.nlm.nih.gov/pubmed/30130634 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.cortex.2018.07.014 |
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