The 15q11.2 BP1-BP2 Microdeletion (<i>Burnside–Butler</i>) Syndrome: In Silico Analyses of the Four Coding Genes Reveal Functional Associations with Neurodevelopmental Phenotypes

The 15q11.2 BP1-BP2 Microdeletion (<i>Burnside–Butler</i>) Syndrome: In Silico Analyses of the Four Coding Genes Reveal Functional Associations with Neurodevelopmental Phenotypes

The 15q11.2 BP1-BP2 microdeletion (<i>Burnside–Butler</i>) syndrome is emerging as the most frequent pathogenic copy number variation (CNV) in humans associated with neurodevelopmental disorders with changes in brain morphology, behavior, and cognition. In this study, we explored functio...

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Bibliographic Details
Main Authors: Syed K. Rafi, Merlin G. Butler
Format: Article
Language:English
Published: MDPI AG 2020-05-01
Series:International Journal of Molecular Sciences
Subjects:
15q11.2 BP1-BP2 deletion (<i>Burnside–Butler</i>) syndrome
<i>NIPA1</i>
<i>NIPA2</i>
<i>CYFIP1</i>
<i>TUBGCP5</i>
Gene Ontology (GO)
Online Access:https://www.mdpi.com/1422-0067/21/9/3296

Internet

https://www.mdpi.com/1422-0067/21/9/3296

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