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A common polymorphism in a Williams syndrome gene predicts amygdala reactivity and extraversion in healthy adults
BACKGROUND: Williams syndrome (WS), a genetic disorder resulting from hemizygous microdeletion of chromosome 7q11.23, has emerged as a model for identifying the genetic architecture of socioemotional behavior. Recently, common polymorphisms in GTF2I, which is found within the WS microdeletion, have...
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| Publicado no: | Biol Psychiatry |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4909599/ https://ncbi.nlm.nih.gov/pubmed/26853120 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.biopsych.2015.12.007 |
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