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Autor:
J C Waltimo, Leena Peltonen, Anders Paetau, P L Lukinmaa, Elina Ikonen, Aarno Palotie, N E Enomaa
Publikováno v:
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society. 41(7)
Aspartylglucosaminidase (AGA: E.C. 3.5.1.26) is a lysosomal amidase that hydrolyzes the N-acetylglucosamine-asparagine linkage as one of the final steps in the breakdown of glycoproteins. Deficiency of this enzyme results in aspartylglucosaminuria (A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c49ce08cd3411127f2c888d56b6aa12e
https://pubmed.ncbi.nlm.nih.gov/7685790
https://pubmed.ncbi.nlm.nih.gov/7685790
