Accumulation of two glycoasparagines in the liver in aspartylglycosaminuria.
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
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1. Glycolipid and Glycoprotein Degradation;Advances in Enzymology - and Related Areas of Molecular Biology;2006-11-22
2. Dissection of the molecular pathology of aspartylglucosammuria provides the basis for DNA diagnostics and future therapeutic interventions;Scandinavian Journal of Clinical and Laboratory Investigation;1993-01
3. Mutations causing aspartylglucosaminuria (AGU): A lysosomal accumulation disease;Human Mutation;1992
4. Glutamyl Ribose-5-Phosphate Storage Disease: Clinical Description and Characterization of the Stored Material;Proceedings in Life Sciences;1985
5. Prenatal diagnosis and fetal pathology of aspartylglucosaminuria;American Journal of Medical Genetics;1984-10
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