Comparison of liver glycosylasparaginases from six vertebrates

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Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1. 1Aspartylglycosaminuria: An inborn error of glycoprotein catabolism1981 · 19 citations
2. 2Aspartylglycosaminuria in the Finnish population: identification of two point mutations in the heavy chain of glycoasparaginase.1991 · 51 citations
3. 3Isolation of a human hepatic 60 kDa aspartylglucosaminidase consisting of three non-identical polypeptides1989 · 22 citations
4. 4Isolation and structure of the core oligosaccharide sequences of IgM1975 · 51 citations
5. 5Characterization of the mutation responsible for aspartylglucosaminuria in three Finnish patients. Amino acid substitution Cys163—-Ser abolishes the activity of lysosomal glycosylasparaginase and its conversion into subunits1991 · 53 citations