Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Epilepsy and HCN1[original query] |
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Mutation analysis of the hyperpolarization-activated cyclic nucleotide-gated channels HCN1 and HCN2 in idiopathic generalized epilepsy. Neurobiology of disease 2008 Jan 29 (1): 59-70. Tang Bin, Sander Thomas, Craven Kimberley B, Hempelmann Anne, Escayg Andr |
Case-control pharmacogenetic study of HCN1/HCN2 variants and genetic generalized epilepsies. Clinical and experimental pharmacology & physiology 2017 Oct . Wu Shu-Zhi, Ye Hua, Yang Xiao-Guo, Lu Zhi-Li, Qu Qiang, Qu Ji |
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 |
The HCN1 p.Ser399Pro variant causes epileptic encephalopathy with super-refractory status epilepticus. Human genome variation 2023 6 10 (1): 20. Yu Kobayashi, Jun Tohyama, Noriyuki Akasaka, Kei Yamada, Moemi Hojo, Eijun Seki, Masaki Miura, Noriko Soma, Takeshi Ono, Mitsuhiro Kato, Mitsuko Nakashima, Hirotomo Saitsu, Naomichi Matsumo |
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- Page last updated:Jun 11, 2024
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