论文信息 - CRISPR/Cas9 facilitates investigation of neural circuit disease using human iPSCs: mechanism of epilepsy caused by an SCN1A loss-of-function mutation - 字舞流文

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

J. Liu | Y. Long | Z. Li | L. Zhang | Yonglong Chen | Xiao-Xin Yan | S. Deng | W. Ma | L. Lai | Y. Shi | W. Chen | C. Gao | X. Yan | X. Guo | H. Zhang | Longmei Zhang | Jiang Liu | Zhiyuan Li | Zhiyuan Li | W. Liao | X. Li | H. Xu | Huijuan Xu | G. Pan | Y. Chen | D. Yu | Sihao Deng | Jiang Liu