CRISPR/Cas9 facilitates investigation of neural circuit disease using human iPSCs: mechanism of epilepsy caused by an SCN1A loss-of-function mutation (Q37347828)
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scientific article published on 05 January 2016
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | CRISPR/Cas9 facilitates investigation of neural circuit disease using human iPSCs: mechanism of epilepsy caused by an SCN1A loss-of-function mutation |
scientific article published on 05 January 2016 |
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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 (English)
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J Liu
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C Gao
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W Chen
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W Ma
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X Li
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Y Shi
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H Zhang
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L Zhang
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Y Long
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H Xu
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X Guo
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S Deng
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X Yan
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D Yu
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G Pan
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Y Chen
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L Lai
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W Liao
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Z Li
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5 January 2016
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e703
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1 January 2016
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