Study of the Impact of Scn1a Gene Mutation on Neural Stem/Progenitor Cells Development in Models of Dravet Syndrome and Potential Therapeutic Strategies.

2019-08-012024-05-17https://scholars.lib.ntu.edu.tw/handle/123456789/688183小兒重度肌痙攣癲癇症候群Scn1a細胞週期神經新生全細胞模式膜箝制Dravet syndromeScn1acell cycleneurogenesiswhole-cell patch clampStudy of the Impact of Scn1a Gene Mutation on Neural Stem/Progenitor Cells Development in Models of Dravet Syndrome and Potential Therapeutic Strategies.