1. Aglago, Elom K, Kim, Andre, Lin, Yi, Tsilidis, Konstantinos K, Campbell, Peter T. . A Genetic Locus within the FMN1/GREM1 Gene Region Interacts with Body Mass Index in Colorectal Cancer Risk. In Cancer research, 83, 2572-2583. doi:10.1158/0008-5472.CAN-22-3713. https://pubmed.ncbi.nlm.nih.gov/37249599/
2. Katoh, Masuko, Katoh, Masaru. . Identification and characterization of the human FMN1 gene in silico. In International journal of molecular medicine, 14, 121-6. doi:. https://pubmed.ncbi.nlm.nih.gov/15202026/
3. Santos, M A, Jimenez, A, Revuelta, J L. . Molecular characterization of FMN1, the structural gene for the monofunctional flavokinase of Saccharomyces cerevisiae. In The Journal of biological chemistry, 275, 28618-24. doi:. https://pubmed.ncbi.nlm.nih.gov/10887197/
4. Patel, Manan V, T S, Chandra. 2019. Metabolic engineering of Ashbya gossypii for enhanced FAD production through promoter replacement of FMN1 gene. In Enzyme and microbial technology, 133, 109455. doi:10.1016/j.enzmictec.2019.109455. https://pubmed.ncbi.nlm.nih.gov/31874696/
5. Al-Qattan, Mohammad M, Alkuraya, Fowzan S. 2018. Cenani-Lenz syndrome and other related syndactyly disorders due to variants in LRP4, GREM1/FMN1, and APC: Insight into the pathogenesis and the relationship to polyposis through the WNT and BMP antagonistic pathways. In American journal of medical genetics. Part A, 179, 266-279. doi:10.1002/ajmg.a.60694. https://pubmed.ncbi.nlm.nih.gov/30569497/
6. Dimitrov, Boyan Ivanov, Voet, Thierry, De Smet, Luc, Fryns, Jean-Pierre, Debeer, Philippe. 2010. Genomic rearrangements of the GREM1-FMN1 locus cause oligosyndactyly, radio-ulnar synostosis, hearing loss, renal defects syndrome and Cenani--Lenz-like non-syndromic oligosyndactyly. In Journal of medical genetics, 47, 569-74. doi:10.1136/jmg.2009.073833. https://pubmed.ncbi.nlm.nih.gov/20610440/
智鼠故事 
