CRISPR/Cas9 facilitates investigation of neural circuit disease using human iPSCs: mechanism of epilepsy caused by an SCN1A loss-of-function mutation
出版年份 2016 全文链接
标题
CRISPR/Cas9 facilitates investigation of neural circuit disease using human iPSCs: mechanism of epilepsy caused by an SCN1A loss-of-function mutation
作者
关键词
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出版物
Translational Psychiatry
Volume 6, Issue 1, Pages e703-e703
出版商
Springer Nature
发表日期
2016-01-05
DOI
10.1038/tp.2015.203
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