Disruption of DDX53 coding sequence has limited impact on iPSC-derived human NGN2 neurons

BACKGROUND: The X-linked PTCHD1 locus is strongly associated with autism spectrum disorder (ASD). Males who carry chromosome microdeletions of PTCHD1 antisense long non-coding RNA (PTCHD1-AS)/DEAD-box helicase 53 (DDX53) have ASD, or a sub-clinical form called Broader Autism Phenotype. If the deleti...

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Detalles Bibliográficos
Autores principales: Faheem, Muhammad, Deneault, Eric, Alexandrova, Roumiana, Rodrigues, Deivid C., Pellecchia, Giovanna, Shum, Carole, Zarrei, Mehdi, Piekna, Alina, Wei, Wei, Howe, Jennifer L., Thiruvahindrapuram, Bhooma, Lamoureux, Sylvia, Ross, P. Joel, Bradley, Clarrisa A., Ellis, James, Scherer, Stephen W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9837974/
https://www.ncbi.nlm.nih.gov/pubmed/36635662
http://dx.doi.org/10.1186/s12920-022-01425-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9837974/
https://www.ncbi.nlm.nih.gov/pubmed/36635662
http://dx.doi.org/10.1186/s12920-022-01425-3

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