1. Beckers, Martin, Stevens, René, Debray, François-Guillaume, Leroy, Patricia. . [Neurodevelopmental impact of a mutation in the RHOBTB2 gene]. In Revue medicale de Liege, 79, 467-470. doi:. https://pubmed.ncbi.nlm.nih.gov/39129541/
2. Tang, Weiwei, Wang, Chuan, Fu, Fangmeng, Chen, Qiang. 2013. RhoBTB2 gene in breast cancer is silenced by promoter methylation. In International journal of molecular medicine, 33, 722-8. doi:10.3892/ijmm.2013.1593. https://pubmed.ncbi.nlm.nih.gov/24356943/
3. Harvey, Susan, King, Mary D, Gorman, Kathleen M. 2021. Paroxysmal Movement Disorders. In Frontiers in neurology, 12, 659064. doi:10.3389/fneur.2021.659064. https://pubmed.ncbi.nlm.nih.gov/34177764/
4. Liu, M, Ding, C H, Chen, C H, Dai, L F, Tian, X J. . [RHOBTB2 gene variation in a child with developmental and epileptic encephalopathy]. In Zhonghua er ke za zhi = Chinese journal of pediatrics, 60, 242-243. doi:10.3760/cma.j.cn112140-20211110-00940. https://pubmed.ncbi.nlm.nih.gov/35240746/
5. Belal, Hazrat, Nakashima, Mitsuko, Matsumoto, Hiroshi, Matsumoto, Naomichi, Saitsu, Hirotomo. 2018. De novo variants in RHOBTB2, an atypical Rho GTPase gene, cause epileptic encephalopathy. In Human mutation, 39, 1070-1075. doi:10.1002/humu.23550. https://pubmed.ncbi.nlm.nih.gov/29768694/
6. Freeman, Scott N, Ma, Yihong, Cress, W Douglas. 2007. RhoBTB2 (DBC2) is a mitotic E2F1 target gene with a novel role in apoptosis. In The Journal of biological chemistry, 283, 2353-62. doi:. https://pubmed.ncbi.nlm.nih.gov/18039672/
7. Mao, Haiting, Qu, Xun, Yang, Yongmei, Sun, Jintang, Zhang, Lining. . A novel tumor suppressor gene RhoBTB2 (DBC2): frequent loss of expression in sporadic breast cancer. In Molecular carcinogenesis, 49, 283-9. doi:10.1002/mc.20598. https://pubmed.ncbi.nlm.nih.gov/19937980/
8. Fonseca, Jacinta, Melo, C, Ferreira, C, Sousa, R, Leão, M. 2021. RHOBTB2 p.Arg511Trp Mutation in Early Infantile Epileptic Encephalopathy-64: Review and Case Report. In Journal of pediatric genetics, 12, 155-158. doi:10.1055/s-0040-1722288. https://pubmed.ncbi.nlm.nih.gov/37090824/
9. Defo, Antoine, Verloes, Alain, Elenga, Narcisse. 2022. Developmental and epileptic encephalopathy related to a heterozygous variant of the RHOBTB2 gene: A case report from French Guiana. In Molecular genetics & genomic medicine, 10, e1929. doi:10.1002/mgg3.1929. https://pubmed.ncbi.nlm.nih.gov/35315256/
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