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题名: CRISPR/Cas9 facilitates investigation of neural circuit disease using human iPSCs: mechanism of epilepsy caused by an SCN1A loss-of-function mutation
作者: 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.
发表日期: 2016
Appears in Collections:华南干细胞与再生医学研究所_期刊论文

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Recommended Citation:
Liu, J.,Gao, C.,Chen, W.,et al. Crispr/cas9 Facilitates Investigation Of Neural Circuit Disease Using Human Ipscs: Mechanism Of Epilepsy Caused By An Scn1a Loss-of-function Mutation[J]. Translational Psychiatry,2016,6.

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