The contribution of GTF2I haploinsufficiency to Williams syndrome

The contribution of GTF2I haploinsufficiency to Williams syndrome

© 2018 Elsevier Ltd Williams syndrome (WS) is a neurodevelopmental disorder involving hemideletion of as many as 26–28 genes, resulting in a constellation of unique physical, cognitive and behavior phenotypes. The haploinsufficiency effect of each gene has been studied and correlated with phenotype(...

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Bibliographic Details
Main Authors: Thanathom Chailangkarn, Chalongrat Noree, Alysson R. Muotri
Other Authors: University of California, San Diego, School of Medicine
Format: Review
Published: 2019
Subjects:
Biochemistry, Genetics and Molecular Biology
Online Access:https://repository.li.mahidol.ac.th/handle/123456789/45099
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Institution: Mahidol University

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https://repository.li.mahidol.ac.th/handle/123456789/45099

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