Liu, J., Gao, C., Chen, W., Ma, W., Li, X., Shi, Y., . . . Li, Z. (2016). CRISPR/Cas9 facilitates investigation of neural circuit disease using human iPSCs: Mechanism of epilepsy caused by an SCN1A loss-of-function mutation. Nature Publishing Group.
Chicago Style CitationLiu, J., et al. CRISPR/Cas9 Facilitates Investigation of Neural Circuit Disease Using Human IPSCs: Mechanism of Epilepsy Caused By an SCN1A Loss-of-function Mutation. Nature Publishing Group, 2016.
MLA CitationLiu, J., et al. CRISPR/Cas9 Facilitates Investigation of Neural Circuit Disease Using Human IPSCs: Mechanism of Epilepsy Caused By an SCN1A Loss-of-function Mutation. Nature Publishing Group, 2016.
Warning: These citations may not always be 100% accurate.