APA

Xie Y., Ng N. N., Safrina O. S., Ramos C. M., Ess K. C., Schwartz P. H., Smith M. A. & O'Dowd D. K. (20210113). Comparisons of dual isogenic human iPSC pairs identify functional alterations directly caused by an epilepsy associated SCN1A mutation. : Neurobiology of disease.

Chicago

Xie Yunyao, Ng Nathan N, Safrina Olga S, Ramos Carmen M, Ess Kevin C, Schwartz Philip H, Smith Martin A and O'Dowd Diane K. 20210113. Comparisons of dual isogenic human iPSC pairs identify functional alterations directly caused by an epilepsy associated SCN1A mutation. : Neurobiology of disease.

Harvard

Xie Y., Ng N. N., Safrina O. S., Ramos C. M., Ess K. C., Schwartz P. H., Smith M. A. and O'Dowd D. K. (20210113). Comparisons of dual isogenic human iPSC pairs identify functional alterations directly caused by an epilepsy associated SCN1A mutation. : Neurobiology of disease.

MLA

Xie Yunyao, Ng Nathan N, Safrina Olga S, Ramos Carmen M, Ess Kevin C, Schwartz Philip H, Smith Martin A and O'Dowd Diane K. Comparisons of dual isogenic human iPSC pairs identify functional alterations directly caused by an epilepsy associated SCN1A mutation. : Neurobiology of disease. 20210113.