2 Article(s)Download |
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PMID | Title | Pub. Year | #Total Relationships |
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| 1 | 25966638 | A novel phenotype in N-glycosylation disorders: Gillessen-Kaesbach-Nishimura skeletal dysplasia due to pathogenic variants in ALG9. | 2016 Feb | 1 | ||
| 2 | 15148656 | Identification and functional analysis of a defect in the human ALG9 gene: definition of congenital disorder of glycosylation type IL. | 2004 Jul | 1 | ||