Dorsal visual stream and LIMK1: hemideletion, haplotype, and enduring effects in children with Williams syndrome

BACKGROUND: Williams syndrome (WS), a rare neurodevelopmental disorder caused by hemizygous deletion of ~ 25 genes from chromosomal band 7q11.23, affords an exceptional opportunity to study associations between a well-delineated genetic abnormality and a well-characterized neurobehavioral profile. C...

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Detalles Bibliográficos
Autores principales: Kippenhan, J. Shane, Gregory, Michael D., Nash, Tiffany, Kohn, Philip, Mervis, Carolyn B., Eisenberg, Daniel P., Garvey, Madeline H., Roe, Katherine, Morris, Colleen A., Kolachana, Bhaskar, Pani, Ariel M., Sorcher, Leah, Berman, Karen F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10464045/
https://www.ncbi.nlm.nih.gov/pubmed/37633900
http://dx.doi.org/10.1186/s11689-023-09493-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10464045/
https://www.ncbi.nlm.nih.gov/pubmed/37633900
http://dx.doi.org/10.1186/s11689-023-09493-x

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