Generation of a human iPSC line CIPi001-A from a benign familial infantile epilepsy patient related 16p11.2 deletion
Summary
The features of 16p11.2 deletion phenotype is developmental delay, intellectual disability, and autism spectrum disorder. Seizures are observed in approximately 20% of individuals with the microdeletion. Induced pluripotent stem cells (iPSCs) were generated from erythroblasts obtained from a child diagnosed with benign familial infantile epilepsy, caused by 16p11.2 deletion. These iPSCs exhibited stable amplification, expressed pluripotent markers, and differentiated spontaneously into three germ layers in vitro. Copyright © 2022 The Authors. Published by Elsevier B.V. All rights reserved.
| Authors | Ji X, Gao Y, Zhang P, Jin Z, Zhang Y, Yang M, Zhang X, Chen Q |
|---|---|
| Journal | Stem cell research |
| Publication Date | 2022 Mar;59:102634 |
| PubMed | 34995844 |
| DOI | 10.1016/j.scr.2021.102634 |