1. Katoh, Masuko, Katoh, Masaru. . Characterization of FMN2 gene at human chromosome 1q43. In International journal of molecular medicine, 14, 469-74. doi:. https://pubmed.ncbi.nlm.nih.gov/15289902/
2. Yamada, Kayo, Ono, Motoharu, Bensaddek, Dalila, Lamond, Angus I, Rocha, Sonia. 2013. FMN2 is a novel regulator of the cyclin-dependent kinase inhibitor p21. In Cell cycle (Georgetown, Tex.), 12, 2348-54. doi:10.4161/cc.25511. https://pubmed.ncbi.nlm.nih.gov/23839046/
3. Li, Jie, Peng, Tianliu, Wang, Le, Xiao, Hongmei, Shi, Xiaobo. 2022. Heterozygous FMN2 missense variant found in a family case of premature ovarian insufficiency. In Journal of ovarian research, 15, 31. doi:10.1186/s13048-022-00960-y. https://pubmed.ncbi.nlm.nih.gov/35227295/
4. Ryley, David A, Wu, Hsin-Hung, Leader, Benjamin, Reindollar, Richard H, Gray, Mark R. . Characterization and mutation analysis of the human formin-2 (FMN2) gene in women with unexplained infertility. In Fertility and sterility, 83, 1363-71. doi:. https://pubmed.ncbi.nlm.nih.gov/15866570/
5. Li, Dao-Jiang, Feng, Zhi-Cai, Li, Xiao-Rong, Hu, Gui. . Involvement of methylation-associated silencing of formin 2 in colorectal carcinogenesis. In World journal of gastroenterology, 24, 5013-5024. doi:10.3748/wjg.v24.i44.5013. https://pubmed.ncbi.nlm.nih.gov/30510376/
6. Gorukmez, Orhan, Gorukmez, Ozlem, Ekici, Arzu. 2020. A Novel Nonsense FMN2 Mutation in Nonsyndromic Autosomal Recessive Intellectual Disability Syndrome. In Fetal and pediatric pathology, 40, 702-706. doi:10.1080/15513815.2020.1737991. https://pubmed.ncbi.nlm.nih.gov/32162566/
7. Charfi, Cyndia, Voisin, Véronique, Levros, Louis-Charles, Edouard, Elsy, Rassart, Eric. 2010. Gene profiling of Graffi murine leukemia virus-induced lymphoid leukemias: identification of leukemia markers and Fmn2 as a potential oncogene. In Blood, 117, 1899-910. doi:10.1182/blood-2010-10-311001. https://pubmed.ncbi.nlm.nih.gov/21135260/
智鼠故事 
