Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Ataxia and SCN1A[original query] |
---|
Genetic Variants Associated with Episodic Ataxia in Korea. Scientific reports 2017 10 7 (1): 13855. Choi Kwang-Dong, Kim Ji-Soo, Kim Hyo-Jung, Jung Ileok, Jeong Seong-Hae, Lee Seung-Han, Kim Dong Uk, Kim Sang-Ho, Choi Seo Young, Shin Jin-Hong, Kim Dae-Seong, Park Kyung-Pil, Kim Hyang-Sook, Choi Jae-Hw |
Gene mutational analysis in a cohort of Chinese children with unexplained epilepsy: Identification of a new KCND3 phenotype and novel genes causing Dravet syndrome. Seizure 2019 2 66 26-30. Wang Jiaping, Wen Yongxin, Zhang Qingping, Yu Shujie, Chen Yan, Wu Xiru, Zhang YueHua, Bao Xinh |
Possible Genetic Determinants of Response to Phenytoin in a Group of Colombian Patients With Epilepsy. Frontiers in pharmacology 2020 11 555. Calderon-Ospina Carlos Alberto, Galvez Jubby Marcela, López-Cabra Claudia, Morales Natalia, Restrepo Carlos Martín, Rodríguez Jesús, Aristizábal-Gutiérrez Fabio Ancízar, Velez-van-Meerbeke Alberto, Laissue Paul, Fonseca-Mendoza Dora Jane |
Use of perampanel in children with refractory epilepsy of genetic aetiology. Epileptic disorders : international epilepsy journal with videotape 2022 6 24 (4): 687-695. Qu Rui, Dai Yuanyuan, Qu Xiangju, Li Yan, Shao Xuejun, Zhou Rui, Zhu Yali, Chen Xuq |
- Page last reviewed:Feb 1, 2024
- Content source: