Dissecting developmental disorders caused by CTCF mutation at R567 [snRNA-seq]. Dissecting developmental disorders caused by CTCF mutation at R567 [snRNA-seq]
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资源简介：
In this study, we performed single nucleus RNA sequencing in heart, lung and cortex tissues from E18.5 mouse embryo. Overall design: SnRNA-seq was performed using wild type and Ctcf homozygous mutated heart, lung and cortex tissues from E18.5 mouse embryo.
创建时间：
2022-10-03
