1. Zhu, Ze-Yu, Li, Zi-Yi, Zhang, Chao, Tian, Wo-Tu, Cao, Li. 2022. A novel homozygous mutation in ERLIN1 gene causing spastic paraplegia 62 and literature review. In European journal of medical genetics, 65, 104608. doi:10.1016/j.ejmg.2022.104608. https://pubmed.ncbi.nlm.nih.gov/36100157/
2. Feitosa, Mary F, Wojczynski, Mary K, North, Kari E, Carr, Jeffrey J, Borecki, Ingrid B. 2013. The ERLIN1-CHUK-CWF19L1 gene cluster influences liver fat deposition and hepatic inflammation in the NHLBI Family Heart Study. In Atherosclerosis, 228, 175-80. doi:10.1016/j.atherosclerosis.2013.01.038. https://pubmed.ncbi.nlm.nih.gov/23477746/
3. Cogan, Guillaume, Zaki, Maha S, Issa, Mahmoud, de Sainte Agathe, Jean-Madeleine, Mignot, Cyril. 2024. Biallelic variants in ERLIN1: a series of 13 individuals with spastic paraparesis. In Human genetics, 143, 1353-1362. doi:10.1007/s00439-024-02702-0. https://pubmed.ncbi.nlm.nih.gov/39367212/
4. Huang, Susie S Y, Toufiq, Mohammed, Saraiva, Luis R, Chaussabel, Damien, Garand, Mathieu. 2021. Transcriptome and Literature Mining Highlight the Differential Expression of ERLIN1 in Immune Cells during Sepsis. In Biology, 10, . doi:10.3390/biology10080755. https://pubmed.ncbi.nlm.nih.gov/34439987/
5. Rendel, Miriam Daphne, Vitali, Cecilia, Creasy, Kate Townsend, Rader, Daniel J, Schneider, Carolin Victoria. 2024. The common p.Ile291Val variant of ERLIN1 enhances TM6SF2 function and is associated with protection against MASLD. In Med (New York, N.Y.), 5, 963-980.e5. doi:10.1016/j.medj.2024.04.010. https://pubmed.ncbi.nlm.nih.gov/38776916/
6. Chang, Lijia, Wang, Tong, Qu, Youge, Wei, Yan, Hashimoto, Kenji. 2024. Identification of novel endoplasmic reticulum-related genes and their association with immune cell infiltration in major depressive disorder. In Journal of affective disorders, 356, 190-203. doi:10.1016/j.jad.2024.04.029. https://pubmed.ncbi.nlm.nih.gov/38604455/
智鼠故事 
