CRISPR/Cas9 facilitates investigation of neural circuit disease using human iPSCs: mechanism of epilepsy caused by an SCN1A loss-of-function mutation
文献类型：期刊论文
| 作者 | Li, Z.; Liu, J.; Gao, C.; Chen, W.; Ma, W.; Li, X.; Shi, Y.; Zhang, H.; Zhang, L.; Long, Y. |
| 刊名 | TRANSLATIONAL PSYCHIATRY
 |
| 出版日期 | 2016 |
| 卷号 | 6 |
| ISSN号 | 2158-3188 |
| 学科主题 | Psychiatry |
| 语种 | 英语 |
| 源URL | [http://ir.foo.ac.cn/handle/2SETSVCV/488]  |
| 专题 | 中国科学院广州生物医药与健康研究院 |
| 推荐引用方式 GB/T 7714 | Li, Z.,Liu, J.,Gao, C.,et al. CRISPR/Cas9 facilitates investigation of neural circuit disease using human iPSCs: mechanism of epilepsy caused by an SCN1A loss-of-function mutation[J]. TRANSLATIONAL PSYCHIATRY,2016,6. |
| APA | Li, Z..,Liu, J..,Gao, C..,Chen, W..,Ma, W..,...&Liao, W..(2016).CRISPR/Cas9 facilitates investigation of neural circuit disease using human iPSCs: mechanism of epilepsy caused by an SCN1A loss-of-function mutation.TRANSLATIONAL PSYCHIATRY,6. |
| MLA | Li, Z.,et al."CRISPR/Cas9 facilitates investigation of neural circuit disease using human iPSCs: mechanism of epilepsy caused by an SCN1A loss-of-function mutation".TRANSLATIONAL PSYCHIATRY 6(2016). |
入库方式： OAI收割
来源：广州生物医药与健康研究院
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