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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...

Täydet tiedot

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Bibliografiset tiedot
Julkaisussa:BMC Neurosci
Päätekijät: Crespi, Bernard J, Hurd, Peter L
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BioMed Central 2014
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC4247780/
https://ncbi.nlm.nih.gov/pubmed/25429715
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12868-014-0127-1
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