Comparisons of dual isogenic human iPSC pairs identify functional alterations directly caused by an epilepsy associated SCN1A mutation.

Xie Y, Ng NN, Safrina OS, Ramos CM, Ess KC, Schwartz PH, Smith MA, O'Dowd DK
Neurobiol Dis. 2020 Feb;134:104627. doi: 10.1016/j.nbd.2019.104627. Epub 2019 Nov 28. PubMed Article

Plasmids from Article

No plasmids are currently publicly available from Addgene for this article.