Comparisons of dual isogenic human iPSC pairs identify functional alterations directly caused by an epilepsy associated SCN1A mutation
Yunyao Xie, Nathan Norton Ng, Olga Safrina, Carmen M. Ramos, Kevin C. Ess, Philip H. Schwartz, Martin A. Smith, Diane K. O’Dowd
The paper compares dual isogenic human iPSC pairs to identify functional alterations caused by an epilepsy-associated SCN1A mutation and its interaction with genetic background.
Neurobiology of Disease · Nov 28, 2019Peer-reviewedNeuroscience