HuGE Literature Finder
Records 1-3
Genetic Variants Identified from Epilepsy of Unknown Etiology in Chinese Children by Targeted Exome Sequencing.
Scientific reports 2017 Jan 7 40319. Wang Yimin, Du Xiaonan, Bin Rao, Yu Shanshan, Xia Zhezhi, Zheng Guo, Zhong Jianmin, Zhang Yunjian, Jiang Yong-Hui, Wang |
SCN1A variations and response to multiple antiepileptic drugs.
The pharmacogenomics journal 2014 Aug 14 (4): 385-9. Yip T S C, O'Doherty C, Tan N C K, Dibbens L M, Suppiah |
A role of SCN9A in human epilepsies, as a cause of febrile seizures and as a potential modifier of Dravet syndrome.
PLoS genetics 2009 Sep 5 (9): e1000649. Singh Nanda A, Pappas Chris, Dahle E Jill, Claes Lieve R F, Pruess Timothy H, De Jonghe Peter, Thompson Joel, Dixon Missy, Gurnett Christina, Peiffer Andy, White H Steve, Filloux Francis, Leppert Mark |
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- Page last updated:Apr 21, 2021
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