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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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  • Release time:2016-04-02

  • Journal:Transl Psychiatry

  • Co-author: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

  • Document Type:J

  • Volume:6

  • Page Number:e703

  • Translation or Not:yes

  • Date of Publication:2016-01-05

  • Links to published journals:http://www.ncbi.nlm.nih.gov/pubmed/26731440

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    • Attachments:

  • 2016-transl-Pschyiatry.pdf   
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