1. Tadmouri, Abir, Kiyonaka, Shigeki, Barbado, Maud, Mori, Yasuo, De Waard, Michel. 2012. Cacnb4 directly couples electrical activity to gene expression, a process defective in juvenile epilepsy. In The EMBO journal, 31, 3730-44. doi:10.1038/emboj.2012.226. https://pubmed.ncbi.nlm.nih.gov/22892567/
2. Ohmori, Iori, Ouchida, Mamoru, Miki, Takafumi, Mori, Yasuo, Matsui, Hideki. 2008. A CACNB4 mutation shows that altered Ca(v)2.1 function may be a genetic modifier of severe myoclonic epilepsy in infancy. In Neurobiology of disease, 32, 349-54. doi:10.1016/j.nbd.2008.07.017. https://pubmed.ncbi.nlm.nih.gov/18755274/
3. Coste de Bagneaux, Pierre, von Elsner, Leonie, Bierhals, Tatjana, Flucher, Bernhard E, Kutsche, Kerstin. 2020. A homozygous missense variant in CACNB4 encoding the auxiliary calcium channel beta4 subunit causes a severe neurodevelopmental disorder and impairs channel and non-channel functions. In PLoS genetics, 16, e1008625. doi:10.1371/journal.pgen.1008625. https://pubmed.ncbi.nlm.nih.gov/32176688/
4. Parker, Emily M, Kindja, Nathan L, DeGiosio, Rebecca A, Cheng, Bin, Sweet, Robert A. 2024. Impacts of CACNB4 overexpression on dendritic spine density in both sexes and relevance to schizophrenia. In Translational psychiatry, 14, 484. doi:10.1038/s41398-024-03181-7. https://pubmed.ncbi.nlm.nih.gov/39632796/
5. Naseer, Muhammad Imran, Abdulkareem, Angham Abdulrhman, Rasool, Mahmood, Muthaffar, Osama Yousef, Pushparaj, Peter Natesan. 2022. Whole-Exome Sequencing Identifies Novel SCN1A and CACNB4 Genes Mutations in the Cohort of Saudi Patients With Epilepsy. In Frontiers in pediatrics, 10, 919996. doi:10.3389/fped.2022.919996. https://pubmed.ncbi.nlm.nih.gov/35813387/
6. Rima, Mohamad, Daghsni, Marwa, Lopez, Anaïs, De Waard, Michel, Ronjat, Michel. 2017. Down-regulation of the Wnt/β-catenin signaling pathway by Cacnb4. In Molecular biology of the cell, 28, 3699-3708. doi:10.1091/mbc.E17-01-0076. https://pubmed.ncbi.nlm.nih.gov/29021340/
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