Cargando…
Cognitive-behavioral phenotypes of Williams syndrome are associated with genetic variation in the GTF2I gene, in a healthy population
BACKGROUND: Individuals with Williams syndrome, a neurogenetic condition caused by deletion of a set of genes at chromosomal location 7q11.23, exhibit a remarkable suite of traits including hypersociality with high, nonselective friendliness and low social anxiety, expressive language relatively wel...
Autores principales: | Crespi, Bernard J, Hurd, Peter L |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4247780/ https://www.ncbi.nlm.nih.gov/pubmed/25429715 http://dx.doi.org/10.1186/s12868-014-0127-1 |
Ejemplares similares
-
Consistent hypersocial behavior in mice carrying a deletion of Gtf2i but no evidence of hyposocial behavior with Gtf2i duplication: Implications for Williams–Beuren syndrome and autism spectrum disorder
por: Martin, Loren A., et al.
Publicado: (2017) -
Variation in the Williams syndrome GTF2I gene and anxiety proneness interactively affect prefrontal cortical response to aversive stimuli
por: Jabbi, M, et al.
Publicado: (2015) -
A Role for Transcription Factor GTF2IRD2 in Executive Function in Williams-Beuren Syndrome
por: Porter, Melanie A., et al.
Publicado: (2012) -
TFII-I/Gtf2i and Erythro-Megakaryopoiesis
por: Gurumurthy, Aishwarya, et al.
Publicado: (2020) -
Association of GTF2IRD1–GTF2I polymorphisms with neuromyelitis optica spectrum disorders in Han Chinese patients
por: Xie, Jing-Lu, et al.
Publicado: (2019)