Isolation of a human hepatic 60 kDa aspartylglucosaminidase consisting of three non-identical polypeptides.

We have characterized the properties of human aspartylglucosaminidase (EC 3.5.1.26), the lysosomal enzyme which is deficient in the human inherited disease aspartylglucosaminuria. The purification procedure from human liver included affinity chromatography, gel filtration, strong-anion- and strong-c...

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Bibliografiska uppgifter
Huvudupphovsmän: Baumann, M, Peltonen, L, Aula, P, Kalkkinen, N
Materialtyp: Artigo
Språk:Inglês
Publicerad: 1989
Ämnen:
Research Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC1133246/
https://ncbi.nlm.nih.gov/pubmed/2818562
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