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aspartylglucosaminuria
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AGA
Human aspartylglucosaminidase. A biochemical and immunocytochemical characterization of the enzyme in normal and aspartylglucosaminuria fibroblasts
Aspartylglucosaminuria: cDNA encoding human aspartylglucosaminidase and the missense mutation causing the disease
Chromosomal localization of the human glycoasparaginase gene to 4q32-q33
In vitro mutagenesis helps to unravel the biological consequences of aspartylglucosaminuria mutation
Genomic structure of human lysosomal glycosylasparaginase
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