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

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

Abstract 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 pr...

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Bibliographic Details
Main Authors: J. Shane Kippenhan, Michael D. Gregory, Tiffany Nash, Philip Kohn, Carolyn B. Mervis, Daniel P. Eisenberg, Madeline H. Garvey, Katherine Roe, Colleen A. Morris, Bhaskar Kolachana, Ariel M. Pani, Leah Sorcher, Karen F. Berman
Format: Article
Language:English
Published: BMC 2023-08-01
Series:Journal of Neurodevelopmental Disorders
Subjects:
Williams syndrome
Hemideletion
LIMK1
Dorsal stream
Intraparietal sulcus
Online Access:https://doi.org/10.1186/s11689-023-09493-x

Internet

https://doi.org/10.1186/s11689-023-09493-x

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