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

Descriptively quantitative relationship between mutated N-acetylgalactosamine-6-sulfatase and mucopolysaccharidosis IVA.

Biopolymers - 1 Jan 2009

Yan Shaomin, Wu Guang

Abstract excerpt

To study the quantitative relationship between the mutant N-acetylgalactosamine-6-sulfatase and the occurrence of mucopolysaccharidosis IVA, the human N-acetylgalactosamine-6-sulfatase with 117 mutations was quantified using the amino-acid distribution probability, then the mutations and clinical outcomes were coupled using the cross-impact analysis. The results show that a patient has 0.94 chance of being...

Read the complete abstract on PubMed

Topics

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

Share to Cysteine
Share to Genetic Predisposition to Disease
Share to Mucopolysaccharidosis IV

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Source

Identifiers

PMID: 19373925
DOI: 10.1002/bip.21205

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.

Research trail→

Click a neighbor to travelStep 1 · 10 closest

Descriptively quantitative relationship between mutated N-acetylgalactosamine-6-sulfatase and mucopolysaccharidosis IVA.PMID 19373925Read ↗

Quantitative relationship between mutated amino-acid sequence of human copper-transporting ATPases and their related diseases.Semantic proximity Read ↗

Connecting mutant phenylalanine hydroxylase with phenylketonuria.Semantic proximity Read ↗

Linking mutated primary structure of adrenoleukodystrophy protein with X-linked adrenoleukodystrophy.Semantic proximity Read ↗

Mutation patterns in human alpha-galactosidase A.Semantic proximity Read ↗

Prediction of mutation trend in hemagglutinins and neuraminidases from influenza A viruses by means of cross-impact analysis.Semantic proximity Read ↗

Determination of mutation pattern in human androgen receptor by means of amino-acid pair predictability.Semantic proximity Read ↗

Generalized pairwise comparisons of prioritized outcomes are a powerful and patient-centric analysis of multi-domain scoresSemantic proximity Read ↗

Determination of amino acid pairs sensitive to variants in human beta-glucocerebrosidase by means of a random approach.Semantic proximity Read ↗

A statistical theory of amino acid mutation.Semantic proximity Read ↗

A phenotypically neutral dimorphism of protein S: the substitution of Lys155 by Glu in the second EGF domain predicted by an A to G base exchange in the gene.Semantic proximity Read ↗

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