Dissecting 16p11.2 hemi-deletion to study sex-specific striatal phenotypes of neurodevelopmental disorders

Neurodevelopmental disorders (NDDs) are polygenic in nature and copy number variants (CNVs) are ideal candidates to study the nature of this polygenic risk. The disruption of striatal circuits is considered a central mechanism in NDDs. The 16p11.2 hemi-deletion (16p11.2 del) is one of the most commo...

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Detalles Bibliográficos
Autores principales: Abel, Ted, Kim, Jaekyoon, Vanrobaeys, Yann, Peterson, Zeru, Kelvington, Benjamin, Gaine, Marie, Nickl-Jockschat, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Journal Experts 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9949238/
https://www.ncbi.nlm.nih.gov/pubmed/36824977
http://dx.doi.org/10.21203/rs.3.rs-2565823/v1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9949238/
https://www.ncbi.nlm.nih.gov/pubmed/36824977
http://dx.doi.org/10.21203/rs.3.rs-2565823/v1

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