Study on the effects of Scn1a mutation (Dravet syndrome) in neurogenesis
碩士 === 國立臺灣大學 === 藥理學研究所 === 103 === Dravet syndrome is a refractory seizure characterized by severe infant-onset myoclonic epilepsy, delayed psychomotor development and autism-spectrum behaviours. Loss-of-function mutations in Scn1a gene which encodes the type Ⅰvoltage-gated sodium channel (Nav1.1)...
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| Format: | Others |
| Language: | zh-TW |
| Published: |
2015
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| Online Access: | http://ndltd.ncl.edu.tw/handle/71846580913041455264 |