CRISPR/Cas9 facilitates investigation of neural circuit disease using human iPSCs: mechanism of epilepsy caused by an SCN1A loss-of-function mutation.
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.
Liu J, et al. Among authors: shi y.
Transl Psychiatry. 2016 Jan 5;6(1):e703. doi: 10.1038/tp.2015.203.
Transl Psychiatry. 2016.
PMID: 26731440
Free PMC article.