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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Detalles Bibliográficos
Autores principales: Rafi, Syed K., Butler, Merlin G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7246448/
https://www.ncbi.nlm.nih.gov/pubmed/32384786
http://dx.doi.org/10.3390/ijms21093296

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7246448/
https://www.ncbi.nlm.nih.gov/pubmed/32384786
http://dx.doi.org/10.3390/ijms21093296

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