CRISPR/Cas9 facilitates investigation of neural circuit disease using human iPSCs: mechanism of epilepsy caused by an SCN1A loss-of-function mutation

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发表刊物：Transl Psychiatry

合写作者：Yu, Yan X, Deng S, Guo X, Xu H, Long Y, Zhang L, Zhang H, Shi Y, Li X, Ma W, Chen W, Gao C, Liu L

文献类型：J

卷号：6

页面范围：e703

是否译文：是

发布期刊链接：http://www.ncbi.nlm.nih.gov/pubmed/26731440

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