| Health / Medical Topics |
Aspartylglycosaminuria
A rare autosomal recessive lysosomal disorder characterized by deficiency of N-aspartyl-beta-glucosaminidase. It is characterized by developmental delays during childhood. (NCI Thesaurus)
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A non-essential amino acid in humans, Aspartic Acid has an overall negative charge and plays an important role in the synthesis of…
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A quantitative measurement of aspartate aminotransferase present in a sample.
