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Social Brain Development in Williams Syndrome: The Current Status and Directions for Future Research
Williams syndrome (WS) is a neurodevelopmental condition that occurs as a result of a contiguous deletion of ∼26–28 genes on chromosome 7q11.23. WS is often associated with a distinctive social phenotype characterized by an increased affinity toward processing faces, reduced sensitivity to fear rela...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Frontiers Research Foundation
2012
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3370330/ https://www.ncbi.nlm.nih.gov/pubmed/22701108 http://dx.doi.org/10.3389/fpsyg.2012.00186 |