1. Xue, Yan, Zhao, Yiran, Wu, Bo, Yu, Xiaoli, Cai, Chunquan. 2023. A novel variant in ALG1 gene associated with congenital disorder of glycosylation: A case report and short literature review. In Molecular genetics & genomic medicine, 11, e2197. doi:10.1002/mgg3.2197. https://pubmed.ncbi.nlm.nih.gov/37204045/
2. Budhraja, Rohit, Joshi, Neha, Radenkovic, Silvia, Morava, Eva, Pandey, Akhilesh. 2024. Dysregulated proteome and N-glycoproteome in ALG1-deficient fibroblasts. In Proteomics, 24, e2400012. doi:10.1002/pmic.202400012. https://pubmed.ncbi.nlm.nih.gov/38470198/
3. Öncül, Ümmühan, Kose, Engin, Eminoğlu, Fatma Tuba. 2021. ALG1-CDG: A Patient with a Mild Phenotype and Literature Review. In Molecular syndromology, 13, 69-74. doi:10.1159/000517797. https://pubmed.ncbi.nlm.nih.gov/35221878/
4. Duan, Ye, Li, Li, Panzade, Ganesh Prabhakar, Zinovyeva, Anna, Ambros, Victor. 2024. Modeling neurodevelopmental disorder-associated human AGO1 mutations in Caenorhabditis elegans Argonaute alg-1. In Proceedings of the National Academy of Sciences of the United States of America, 121, e2308255121. doi:10.1073/pnas.2308255121. https://pubmed.ncbi.nlm.nih.gov/38412125/