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Williams syndrome deficits in visual spatial processing linked to GTF2IRD1 and GTF2I on Chromosome 7q11.23

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Year: 2003
Type: article
Source: Genetics in Medicine
DOI: 10.1097/01.gim.0000076975.10224.67
Authors: Hamao Hirota, Rumiko Matsuoka, Xiao-Ning Chen, Lora S. Salandanan, Alan Lincoln, Fredric E. Rose, Mariko Sunahara, Makiko Osawa, Ursula Bellugi, Julie R. Korenberg
Institutions: Cedars-Sinai Medical Center, University of California, Los Angeles, Tokyo Women's Medical University, Alliant University, Salk Institute for Biological Studies
Language: English

Topic: Williams Syndrome Research
Subfield: Developmental Neuroscience
Field: Neuroscience
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: closed

Funders: National Institutes of Health, National Institute of Child Health and Human Development, Eunice Kennedy Shriver National Institute of Child Health and Human Development
Award: Williams Syndrome: A Model for Linking Genes, Neural Systems and Social Phenotype
OpenAlex ID: W2110886936
FWCI: 1.842
Cites: 56
Cited by: 120
Related to: 10
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