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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 5 (of 5 Records)

Query Trace: Epilepsy and HCN2[original query]
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
Augmented currents of an HCN2 variant in patients with febrile seizure syndromes.
Annals of neurology 2010 Apr 67 (4): 542-6.
Dibbens Leanne M, Reid Christopher A, Hodgson Bree, Thomas Evan A, Phillips Alison M, Gazina Elena, Cromer Brett A, Clarke Alison L, Baram Tallie Z, Scheffer Ingrid E, Berkovic Samuel F, Petrou Stev
Gain-of-function HCN2 variants in genetic epilepsy.
Human mutation 2017 Oct .
Li Melody, Maljevic Snezana, Phillips A Marie, Petrovski Slave, Hildebrand Michael S, Burgess Rosemary, Mount Therese, Zara Federico, Striano Pasquale, Schubert Julian, Thiele Holger, Nürnberg Peter, Wong Michael, Weisenberg Judith L, Thio Liu Lin, Lerche Holger, Scheffer Ingrid E, Berkovic Samuel F, Petrou Steven, Reid Christopher
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
Analysis of epilepsy-associated variants in HCN3 - Functional implications and clinical observations.
Epilepsia open 2024 10 .
Peiwei Zhao, Hongbo Xiong, Gunagtao Kuang, Chen Sun, Xiankai Zhang, Yufeng Huang, Sukun Luo, Lei Zhang, Jun Jiang, Xuelian
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