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About this Neuroscience article
CRISPR/Cas9 facilitates investigation of neural circuit disease using human iPSCs: mechanism of epilepsy caused by an SCN1A loss-of-function mutation by Liu, J; Gao, C; Chen, W; Ma, W; Li, X; Shi, Y; Zhang, H; Zhang, L; Long, Y; Xu, H; Guo, X; Deng, S; Yan, X; Yu, D; Pan, G; Chen, Y; Lai, L; Liao, W; Li, Z is a Neuroscience article available to read on EtoBox.
It is typically read by researchers, students, and practitioners in Neuroscience.
- Author
- Liu, J; Gao, C; Chen, W; Ma, W; Li, X; Shi, Y; Zhang, H; Zhang, L; Long, Y; Xu, H; Guo, X; Deng, S; Yan, X; Yu, D; Pan, G; Chen, Y; Lai, L; Liao, W; Li, Z
- Publisher
- Nature Publishing Group; Springer Science and Business Media LLC (ISSN 2158-3188)
- Published
- 2016
- Field
- Neuroscience (Life Sciences)