Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Aspartylglucosaminuria (AGU): protein and gene structure of normal and mutated aspartylglucosaminidase.

Biochemical medicine and metabolic biology - 1 Aug 1993

Halila R, Ikonen E, Tollersrud O, Syvänen A C, Enomaa N, Peltonen L

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Acetylglucosamine
Share to Mutation

Source

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 8373629
DOI: 10.1006/bmmb.1993.1041

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Aspartylglucosaminuria (AGU): protein and gene structure of normal and mutated aspartylglucosaminidase.PMID 8373629Read ↗

Aspartylglycosaminuria: biochemistry and molecular biology.Semantic proximity Read ↗

Molecular pathogenesis of a disease: structural consequences of aspartylglucosaminuria mutations.Semantic proximity Read ↗

Aspartylglycosaminuria: protein chemistry and molecular biology of the most common lysosomal storage disorder of glycoprotein degradation.Semantic proximity Read ↗

Structural basis of aspartylglucosaminuria.Semantic proximity Read ↗

Aspartylglucosaminuria: cDNA encoding human aspartylglucosaminidase and the missense mutation causing the disease.Semantic proximity Read ↗

Dissection of the molecular pathology of aspartylglucosaminuria provides the basis for DNA diagnostics and future therapeutic interventions.Semantic proximity Read ↗

Aspartylglycosaminuria: a review.Semantic proximity Read ↗

Biochemical and structural insights into an allelic variant causing the lysosomal storage disorder - aspartylglucosaminuria.Semantic proximity Read ↗

[A family with two children diagnosed with aspartylglucosaminuria-case report and literature review].Semantic proximity Read ↗

Mutations causing aspartylglucosaminuria (AGU): a lysosomal accumulation disease.Semantic proximity Read ↗

Spectrum of mutations in aspartylglucosaminuria.Semantic proximity Read ↗

A NOVEL ASPARTYLGLUCOSAMINURIA MUTATION IN A PATIENT WITH CO-EXISTENCE OF GAUCHER DISEASE.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.