Human Genome Epidemiology Literature Finder
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Records 1 - 2 (of 2 Records) |
| Query Trace: Disease and HCN2[original query] |
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| 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 |
| 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 |
- Page last reviewed:Feb 1, 2024
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