Single cell analysis of dup15q syndrome reveals developmental and postnatal molecular changes in autism

Duplication 15q (dup15q) syndrome is the most common genetic cause of autism spectrum disorder (ASD). Due to a higher genetic and phenotypic homogeneity compared to idiopathic autism, dup15q syndrome provides a well-defined setting to investigate ASD mechanisms. Previous bulk gene expression studies...

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Detalles Bibliográficos
Autores principales: Perez, Yonatan, Velmeshev, Dmitry, Wang, Li, White, Matthew, Siebert, Clara, Baltazar, Jennifer, Dutton, Natalia Garcia, Wang, Shaohui, Haeussler, Maximilian, Chamberlain, Stormy, Kriegstein, Arnold
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10543006/
https://www.ncbi.nlm.nih.gov/pubmed/37790331
http://dx.doi.org/10.1101/2023.09.22.559056

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10543006/
https://www.ncbi.nlm.nih.gov/pubmed/37790331
http://dx.doi.org/10.1101/2023.09.22.559056

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