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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Bibliografiset tiedot
Julkaisussa:Biol Psychiatry
Päätekijät: Swartz, Johnna R., Waller, Rebecca, Bogdan, Ryan, Knodt, Annchen R., Sabhlok, Aditi, Hyde, Luke W., Hariri, Ahmad R.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2015
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Article
Linkit: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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