1. Boulogne, Floranne, Claus, Laura R, Wiersma, Henry, Franke, Lude, van Eerde, Albertien M. 2023. KidneyNetwork: using kidney-derived gene expression data to predict and prioritize novel genes involved in kidney disease. In European journal of human genetics : EJHG, 31, 1300-1308. doi:10.1038/s41431-023-01296-x. https://pubmed.ncbi.nlm.nih.gov/36807342/
2. Westphal, Vibeke, Xiao, Ming, Kwok, Pui-Yan, Freeze, Hudson H. . Identification of a frequent variant in ALG6, the cause of Congenital Disorder of Glycosylation-Ic. In Human mutation, 22, 420-1. doi:. https://pubmed.ncbi.nlm.nih.gov/14517965/
3. Imbach, T, Burda, P, Kuhnert, P, Berger, E G, Hennet, T. . A mutation in the human ortholog of the Saccharomyces cerevisiae ALG6 gene causes carbohydrate-deficient glycoprotein syndrome type-Ic. In Proceedings of the National Academy of Sciences of the United States of America, 96, 6982-7. doi:. https://pubmed.ncbi.nlm.nih.gov/10359825/
4. Li, Sihong, Li, Zexuan, Wu, Qiuxia, Luo, Xuerong, Shen, Yidong. 2024. Psychiatric assessment and therapy in an adolescent with ALG6-CDG: a six-month follow-up case report. In European child & adolescent psychiatry, 34, 795-800. doi:10.1007/s00787-024-02564-x. https://pubmed.ncbi.nlm.nih.gov/39141102/
5. Monson, Elisha, Cideciyan, Artur V, Roman, Alejandro J, Fliesler, Steven J, Pittler, Steven J. 2024. Inherited Retinal Degeneration Caused by Dehydrodolichyl Diphosphate Synthase Mutation-Effect of an ALG6 Modifier Variant. In International journal of molecular sciences, 25, . doi:10.3390/ijms25021004. https://pubmed.ncbi.nlm.nih.gov/38256083/
6. Drijvers, J M, Lefeber, D J, de Munnik, S A, Wevers, R A, Morava, E. . Skeletal dysplasia with brachytelephalangy in a patient with a congenital disorder of glycosylation due to ALG6 gene mutations. In Clinical genetics, 77, 507-9. doi:10.1111/j.1399-0004.2009.01349.x. https://pubmed.ncbi.nlm.nih.gov/20447155/