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

A new mutant erythrocyte pyrimidine 5'-nucleotidase characterized by fast electrophoretic mobility in a Chinese boy with chronic hemolytic anemia.

Clinica chimica acta; international journal of clinical chemistry - 15 Aug 1991

Li J Y, Wan S D, Ma Z M, Zhao Y H, Zhou G P

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 5'-Nucleotidase
Share to Anemia, Hemolytic
Share to Child
Share to Chronic Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Electrophoresis, Cellulose Acetate

Share to Erythrocytes

Share to Spleen

Share to Uridine Monophosphate

Source

Identifiers

PMID: 1934510
DOI: 10.1016/0009-8981(91)90332-7

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 · 11 closest

A new mutant erythrocyte pyrimidine 5'-nucleotidase characterized by fast electrophoretic mobility in a Chinese boy with chronic hemolytic anemia.PMID 1934510Read ↗

Hereditary erythrocyte pyrimidine 5'-nucleotidase deficiency: a biochemical, genetic and clinical overview.Semantic proximity Read ↗

Functional analysis of pyrimidine 5'-nucleotidase mutants causing nonspherocytic hemolytic anemia.Semantic proximity Read ↗

Molecular basis of pyrimidine 5'-nucleotidase deficiency caused by 3 newly identified missense mutations (c.187T>C, c.469G>C and c.740T>C) and a tabulation of known mutations.Semantic proximity Read ↗

Hereditary pyrimidine 5'-nucleotidase deficiency: from genetics to clinical manifestations.Semantic proximity Read ↗

A rare mutation (p.F149del) of the NT5C3A gene is associated with pyrimidine 5'-nucleotidase deficiency.Semantic proximity Read ↗

Two new mutations of the P5'N-1 gene found in Italian patients with hereditary hemolytic anemia: the molecular basis of the red cell enzyme disorder.Semantic proximity Read ↗

Atypical haemolytic uraemic syndrome in a Japanese patient with DGKE genetic mutations.Semantic proximity Read ↗

Molecular characterization of Turkish patients with pyrimidine 5' nucleotidase-I deficiency.Semantic proximity Read ↗

Genetic basis of hemolytic anemia caused by pyrimidine 5' nucleotidase deficiency.Semantic proximity Read ↗

Molecular basis of Japanese variants of pyrimidine 5'-nucleotidase deficiency.Semantic proximity Read ↗

Altered kinetic property of erythrocyte phosphoribosylpsyrophosphate synthetase in excessive purine production.Semantic proximity Read ↗

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