Genetic contributions to visuospatial cognition in Williams syndrome: insights from two contrasting partial deletion patients

BACKGROUND: Williams syndrome (WS) is a rare neurodevelopmental disorder arising from a hemizygotic deletion of approximately 27 genes on chromosome 7, at locus 7q11.23. WS is characterised by an uneven cognitive profile, with serious deficits in visuospatial tasks in comparison to relatively profic...

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Detalles Bibliográficos
Autores principales: Broadbent, Hannah, Farran, Emily K, Chin, Esther, Metcalfe, Kay, Tassabehji, May, Turnpenny, Peter, Sansbury, Francis, Meaburn, Emma, Karmiloff-Smith, Annette
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4107613/
https://www.ncbi.nlm.nih.gov/pubmed/25057328
http://dx.doi.org/10.1186/1866-1955-6-18

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4107613/
https://www.ncbi.nlm.nih.gov/pubmed/25057328
http://dx.doi.org/10.1186/1866-1955-6-18

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