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

The 15q11.2 BP1-BP2 microdeletion (Burnside–Butler) 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 functions and interactions...

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Detalhes bibliográficos
Publicado no:Int J Mol Sci
Main Authors: Rafi, Syed K., Butler, Merlin G.
Formato: Artigo
Idioma:Inglês
Publicado em: MDPI 2020
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7246448/
https://ncbi.nlm.nih.gov/pubmed/32384786
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms21093296
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