A CRISPR-engineered isogenic model of the 22q11.2 A-B syndromic deletion

22q11.2 deletion syndrome, associated with congenital and neuropsychiatric anomalies, is the most common copy number variant (CNV)-associated syndrome. Patient-derived, induced pluripotent stem cell (iPS) models have provided insight into this condition. However, patient-derived iPS cells may harbor...

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Detalles Bibliográficos
Autores principales: Paranjape, Neha, Lin, Yu-Hsiu T., Flores-Ramirez, Quetzal, Sarin, Vishesh, Johnson, Amanda Brooke, Chu, Julia, Paredes, Mercedes, Wiita, Arun P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10175260/
https://www.ncbi.nlm.nih.gov/pubmed/37169815
http://dx.doi.org/10.1038/s41598-023-34325-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10175260/
https://www.ncbi.nlm.nih.gov/pubmed/37169815
http://dx.doi.org/10.1038/s41598-023-34325-2

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