1. Li, Huajin, Huang, Yanfeng, Li, Jing, Xie, Maosong. 2022. Novel homozygous nonsynonymous variant of CNNM4 gene in a Chinese family with Jalili syndrome. In Molecular genetics & genomic medicine, 10, e1860. doi:10.1002/mgg3.1860. https://pubmed.ncbi.nlm.nih.gov/35150469/
2. Bloch-Zupan, Agnes, Rey, Tristan, Jimenez-Armijo, Alexandra, Bugueno, Isaac Maximiliano, Laugel-Haushalter, Virginie. 2023. Amelogenesis imperfecta: Next-generation sequencing sheds light on Witkop's classification. In Frontiers in physiology, 14, 1130175. doi:10.3389/fphys.2023.1130175. https://pubmed.ncbi.nlm.nih.gov/37228816/
3. Simón, Jorge, Goikoetxea-Usandizaga, Naroa, Serrano-Maciá, Marina, Martínez-Cruz, Luis Alfonso, Martínez-Chantar, María Luz. 2021. Magnesium accumulation upon cyclin M4 silencing activates microsomal triglyceride transfer protein improving NASH. In Journal of hepatology, 75, 34-45. doi:10.1016/j.jhep.2021.01.043. https://pubmed.ncbi.nlm.nih.gov/33571553/
4. Cherkaoui Jaouad, Imane, Lyahyai, Jaber, Guaoua, Soukaina, Boulanouar, Abdelkrim, Sefiani, Abdelaziz. 2017. Novel splice site mutation in CNNM4 gene in a family with Jalili syndrome. In European journal of medical genetics, 60, 239-244. doi:10.1016/j.ejmg.2017.02.004. https://pubmed.ncbi.nlm.nih.gov/28246031/
5. Funato, Yosuke, Yamazaki, Daisuke, Mizukami, Shin, Kikuchi, Kazuya, Miki, Hiroaki. 2014. Membrane protein CNNM4-dependent Mg2+ efflux suppresses tumor progression. In The Journal of clinical investigation, 124, 5398-410. doi:10.1172/JCI76614. https://pubmed.ncbi.nlm.nih.gov/25347473/
6. Daneshmandpour, Yousef, Darvish, Hossein, Pashazadeh, Fariba, Emamalizadeh, Babak. 2019. Features, genetics and their correlation in Jalili syndrome: a systematic review. In Journal of medical genetics, 56, 358-369. doi:10.1136/jmedgenet-2018-105716. https://pubmed.ncbi.nlm.nih.gov/30705057/