1. Erger, Florian, Aryal, Rajindra P, Reusch, Björn, Cummings, Richard D, Beck, Bodo B. 2023. Germline C1GALT1C1 mutation causes a multisystem chaperonopathy. In Proceedings of the National Academy of Sciences of the United States of America, 120, e2211087120. doi:10.1073/pnas.2211087120. https://pubmed.ncbi.nlm.nih.gov/37216524/
2. Li, Gui-Sen, Nie, Guang-Jun, Zhang, Hong, Shen, Yan, Wang, Hai-Yan. 2009. Do the mutations of C1GALT1C1 gene play important roles in the genetic susceptibility to Chinese IgA nephropathy? In BMC medical genetics, 10, 101. doi:10.1186/1471-2350-10-101. https://pubmed.ncbi.nlm.nih.gov/19778426/
3. Crew, Vanja Karamatic, Singleton, Belinda K, Green, Carole, Daniels, Geoff, Anstee, David J. 2008. New mutations in C1GALT1C1 in individuals with Tn positive phenotype. In British journal of haematology, 142, 657-67. doi:10.1111/j.1365-2141.2008.07215.x. https://pubmed.ncbi.nlm.nih.gov/18537974/
4. Xing, Yue, Li, Lina, Zhang, Yaru, Yan, Tiekun, Lin, Shan. 2020. C1GALT1 expression is associated with galactosylation of IgA1 in peripheral B lymphocyte in immunoglobulin a nephropathy. In BMC nephrology, 21, 18. doi:10.1186/s12882-019-1675-5. https://pubmed.ncbi.nlm.nih.gov/31941451/
5. Li, G-S, Zhang, H, Lv, J-C, Shen, Y, Wang, H-Y. 2007. Variants of C1GALT1 gene are associated with the genetic susceptibility to IgA nephropathy. In Kidney international, 71, 448-53. doi:. https://pubmed.ncbi.nlm.nih.gov/17228361/