1. Pujol, Claire, Legrand, Anne, Parodi, Livia, Trifunovic, Aleksandra, Stevanin, Giovanni. 2021. Implication of folate deficiency in CYP2U1 loss of function. In The Journal of experimental medicine, 218, . doi:10.1084/jem.20210846. https://pubmed.ncbi.nlm.nih.gov/34546337/
2. Durand, Christelle M, Dhers, Laura, Tesson, Christelle, Stevanin, Giovanni, Goizet, Cyril. 2017. CYP2U1 activity is altered by missense mutations in hereditary spastic paraplegia 56. In Human mutation, 39, 140-151. doi:10.1002/humu.23359. https://pubmed.ncbi.nlm.nih.gov/29034544/
3. Legrand, A, Pujol, C, Durand, C M, Goizet, C, Albuisson, J. 2021. Pseudoxanthoma elasticum overlaps hereditary spastic paraplegia type 56. In Journal of internal medicine, 289, 709-725. doi:10.1111/joim.13193. https://pubmed.ncbi.nlm.nih.gov/33107650/
4. Devos, Aurore, Lino Cardenas, Christian Lacks, Glowacki, François, Broly, Franck, Cauffiez, Christelle. 2010. Genetic polymorphism of CYP2U1, a cytochrome P450 involved in fatty acids hydroxylation. In Prostaglandins, leukotrienes, and essential fatty acids, 83, 105-10. doi:10.1016/j.plefa.2010.06.005. https://pubmed.ncbi.nlm.nih.gov/20630735/
5. Yu, Xuming, Wu, Juan, Hu, Mingbai, Feng, Yu-Qi, Yue, Jiang. 2019. Glutamate affects the CYP1B1- and CYP2U1-mediated hydroxylation of arachidonic acid metabolism via astrocytic mGlu5 receptor. In The international journal of biochemistry & cell biology, 110, 111-121. doi:10.1016/j.biocel.2019.03.001. https://pubmed.ncbi.nlm.nih.gov/30858141/
智鼠故事 
