1. Vlaskamp, Danique R M, Rump, Patrick, Callenbach, Petra M C, van Ravenswaaij-Arts, Conny M A, Brouwer, Oebele F. 2016. Haploinsufficiency of the STX1B gene is associated with myoclonic astatic epilepsy. In European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society, 20, 489-92. doi:10.1016/j.ejpn.2015.12.014. https://pubmed.ncbi.nlm.nih.gov/26818399/
2. Wolking, Stefan, May, Patrick, Mei, Davide, Lerche, Holger, Schubert, Julian. 2019. Clinical spectrum of STX1B-related epileptic disorders. In Neurology, 92, e1238-e1249. doi:10.1212/WNL.0000000000007089. https://pubmed.ncbi.nlm.nih.gov/30737342/
3. Vardar, Gülçin, Gerth, Fabian, Schmitt, Xiao Jakob, Rosenmund, Christian, Freund, Christian. . Epilepsy-causing STX1B mutations translate altered protein functions into distinct phenotypes in mouse neurons. In Brain : a journal of neurology, 143, 2119-2138. doi:10.1093/brain/awaa151. https://pubmed.ncbi.nlm.nih.gov/32572454/
4. Haag, Carolin, Uysal, Betül, Marquetand, Justus, Lerche, Holger, Schwarz, Niklas. 2023. Generation of an induced pluripotent stem cell (iPSC) line from a patient with GEFS+ carrying a STX1B (p.Lys45delinsArgMetCysIleGlu and p.Leu46Met) mutation. In Stem cell research, 67, 103028. doi:10.1016/j.scr.2023.103028. https://pubmed.ncbi.nlm.nih.gov/36652844/
5. Kofuji, Takefumi, Fujiwara, Tomonori, Sanada, Masumi, Mishima, Tatsuya, Akagawa, Kimio. 2014. HPC-1/syntaxin 1A and syntaxin 1B play distinct roles in neuronal survival. In Journal of neurochemistry, 130, 514-25. doi:10.1111/jnc.12722. https://pubmed.ncbi.nlm.nih.gov/24666284/
6. Wang, Jian-Yong, Gong, Mei-Ying, Ye, Yang-Lie, Zhang, Xiong, Zhu, Jian-Hong. 2014. The RIT2 and STX1B polymorphisms are associated with Parkinson's disease. In Parkinsonism & related disorders, 21, 300-2. doi:10.1016/j.parkreldis.2014.12.006. https://pubmed.ncbi.nlm.nih.gov/25534083/
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