Xie, Yunyao <br/><br/>
Comparisons of dual isogenic human iPSC pairs identify functional alterations directly caused by an epilepsy associated SCN1A mutation.  [electronic resource] 

 -  Neurobiology of disease  02 2020 
 - 104627 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1095-953X 
<br/><br/><label>Standard No.: </label>10.1016/j.nbd.2019.104627  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Epilepsy--genetics<br/>Genotype<br/>Humans<br/>Induced Pluripotent Stem Cells<br/>Mutation<br/>NAV1.1 Voltage-Gated Sodium Channel--genetics<br/>Neurons<br/>Phenotype<br/>Seizures, Febrile--genetics