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2. Fan, Guoyong, Yan, Qian, Chen, Yubin, Gou, Qing, Hou, Baohua. 2024. FLNB overexpression promotes tumor progression and associates with immune suppression, evasion and stemness in pancreatic cancer. In American journal of cancer research, 14, 709-726. doi:. https://pubmed.ncbi.nlm.nih.gov/38455418/
3. Farrington-Rock, Claire, Kirilova, Veneta, Dillard-Telm, Lisa, Cohn, Daniel H, Krakow, Deborah. 2007. Disruption of the Flnb gene in mice phenocopies the human disease spondylocarpotarsal synostosis syndrome. In Human molecular genetics, 17, 631-41. doi:. https://pubmed.ncbi.nlm.nih.gov/17635842/
4. Huang, Wenbin, Zhang, Shiying, Lin, Jiuxiang, Zhao, Huaxiang, Chen, Feng. 2023. Rare loss-of-function variants in FLNB cause non-syndromic orofacial clefts. In Journal of genetics and genomics = Yi chuan xue bao, 51, 222-229. doi:10.1016/j.jgg.2023.03.012. https://pubmed.ncbi.nlm.nih.gov/37003352/
5. Jiang, Heng, Liang, Shulun, He, Kai, Yang, Fu, Zhou, Xuhui. 2020. Exome sequencing analysis identifies frequent oligogenic involvement and FLNB variants in adolescent idiopathic scoliosis. In Journal of medical genetics, 57, 405-413. doi:10.1136/jmedgenet-2019-106411. https://pubmed.ncbi.nlm.nih.gov/32381728/
6. Chakarova, C, Wehnert, M S, Uhl, K, van der Ven, P F, Fürst, D O. . Genomic structure and fine mapping of the two human filamin gene paralogues FLNB and FLNC and comparative analysis of the filamin gene family. In Human genetics, 107, 597-611. doi:. https://pubmed.ncbi.nlm.nih.gov/11153914/
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