1. Liu, Tiezhu, Li, Jiajia, Wang, Xueqi, Wang, Shiwen, Liang, Mifang. 2023. Knockout of CLTC gene reduces but not completely block SFTSV infection. In PloS one, 18, e0285673. doi:10.1371/journal.pone.0285673. https://pubmed.ncbi.nlm.nih.gov/37624798/
2. Bridge, Julia A, Sumegi, Janos, Royce, Thomas, Baker, Michael, Linos, Konstantinos. 2020. A novel CLTC-FOSB gene fusion in pseudomyogenic hemangioendothelioma of bone. In Genes, chromosomes & cancer, 60, 38-42. doi:10.1002/gcc.22891. https://pubmed.ncbi.nlm.nih.gov/32749039/
3. Bayati, Armin, Kumar, Rahul, Francis, Vincent, McPherson, Peter S. 2021. SARS-CoV-2 infects cells after viral entry via clathrin-mediated endocytosis. In The Journal of biological chemistry, 296, 100306. doi:10.1016/j.jbc.2021.100306. https://pubmed.ncbi.nlm.nih.gov/33476648/
4. Hamdan, Fadi F, Myers, Candace T, Cossette, Patrick, Minassian, Berge A, Michaud, Jacques L. . High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies. In American journal of human genetics, 101, 664-685. doi:10.1016/j.ajhg.2017.09.008. https://pubmed.ncbi.nlm.nih.gov/29100083/
5. DeMari, Joseph, Mroske, Cameron, Tang, Sha, Miller, Ryan, Lebel, Robert R. 2016. CLTC as a clinically novel gene associated with multiple malformations and developmental delay. In American journal of medical genetics. Part A, 170A, 958-66. doi:10.1002/ajmg.a.37506. https://pubmed.ncbi.nlm.nih.gov/26822784/
6. Argani, Pedram, Lui, Man Yee, Couturier, Jérôme, Fournet, Jean-Christophe, Ladanyi, Marc. . A novel CLTC-TFE3 gene fusion in pediatric renal adenocarcinoma with t(X;17)(p11.2;q23). In Oncogene, 22, 5374-8. doi:. https://pubmed.ncbi.nlm.nih.gov/12917640/
7. Cheng, Chen, Yang, Fan, Zhao, Sheng, Chen, Xinlin. 2023. A novel de novo CLTC variant altering RNA splicing causes fetal developmental abnormalities. In BMC medical genomics, 16, 331. doi:10.1186/s12920-023-01778-3. https://pubmed.ncbi.nlm.nih.gov/38111042/
8. Murdock, David R, Dai, Hongzheng, Burrage, Lindsay C, Hanchard, Neil A, Lee, Brendan. . Transcriptome-directed analysis for Mendelian disease diagnosis overcomes limitations of conventional genomic testing. In The Journal of clinical investigation, 131, . doi:10.1172/JCI141500. https://pubmed.ncbi.nlm.nih.gov/33001864/
9. Kemps, Paul G, Baelde, Hans J, Vorderman, Ruben H P, van Halteren, Astrid G S, Hogendoorn, Pancras C W. . Recurrent CLTC::SYK fusions and CSF1R mutations in juvenile xanthogranuloma of soft tissue. In Blood, 144, 2439-2455. doi:10.1182/blood.2024025127. https://pubmed.ncbi.nlm.nih.gov/39316650/
智鼠故事 
