| Title | Date | PubMed ID |
|---|
| A novel phenotype in N-glycosylation disorders: Gillessen-Kaesbach-Nishimura skeletal dysplasia due to pathogenic variants in ALG9. | 2016 Feb | 25966638 |
| Evolutionarily conserved glycan signal to degrade aberrant brassinosteroid receptors in Arabidopsis. | 2012 Jul 10 | 22733738 |
| Quality control of glycoproteins bearing truncated glycans in an ALG9-defective (CDG-IL) patient. | 2009 Aug | 19451548 |
| ALG9 mannosyltransferase is involved in two different steps of lipid-linked oligosaccharide biosynthesis. | 2005 Nov | 15987956 |
| CDG-IL: an infant with a novel mutation in the ALG9 gene and additional phenotypic features. | 2005 Jul 15 | 15945070 |
| Identification and functional analysis of a defect in the human ALG9 gene: definition of congenital disorder of glycosylation type IL. | 2004 Jul | 15148656 |