Williams syndrome hemideletion and LIMK1 variation both affect dorsal stream functional connectivity

Williams syndrome is a rare genetic disorder caused by hemizygous deletion of ∼1.6 Mb affecting 26 genes on chromosome 7 (7q11.23) and is clinically typified by two cognitive/behavioural hallmarks: marked visuospatial deficits relative to verbal and non-verbal reasoning abilities and hypersocial per...

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Detalhes bibliográficos
Publicado no:Brain
Main Authors: Gregory, Michael D, Mervis, Carolyn B, Elliott, Maxwell L, Kippenhan, J Shane, Nash, Tiffany, B. Czarapata, Jasmin, Prabhakaran, Ranjani, Roe, Katherine, Eisenberg, Daniel P, Kohn, Philip D, Berman, Karen F
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2019
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Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6906590/
https://ncbi.nlm.nih.gov/pubmed/31687737
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/brain/awz323
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