CTCF mutation at R567 causes developmental disorders by 3D genome rearrangement, premature exhaustion of stem cells and abnormal neurodevelopment [scRNA-seq]
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下载链接：
https://www.ncbi.nlm.nih.gov/sra/SRP436281
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资源简介：
In this study, we performed single RNA sequencing in 1-month and 2-month cortical organoids derived from wild-type and Ctcf heterozygous hESCs. Overall design: ScRNA-seq was performed using cortical organoids derived from wild-type and Ctcf heterozygous hESCs.
创建时间：
2025-04-11
