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...

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Detalles Bibliográficos
Autores principales: Crespi, Bernard J, Hurd, Peter L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Research Article
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

Internet

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

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