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

G6PD deficiency: the genotype-phenotype association.

Blood reviews - 1 Sept 2007

Mason Philip J, Bautista José M, Gilsanz Florinda

Abstract excerpt

Deficiency of glucose-6-phosphate dehydrogenase is a very common X-linked genetic disorder though most deficient people are asymptomatic. A number of different G6PD variants have reached polymorphic frequencies in different parts of the world due to the relative protection they confer against malaria infection. People, usually males, with deficient alleles are susceptible to neonatal jaundice, and acute hemolytic...

Read the complete abstract on PubMed

Topics

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

Share to Anemia, Hemolytic
Share to Chromosomes, Human, X
Share to Disease Susceptibility

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

Share to Genes, X-Linked

Share to Glucosephosphate Dehydrogenase

Share to Glucosephosphate Dehydrogenase Deficiency

Share to Malaria

Share to Point Mutation

Source

Identifiers

PMID: 17611006
DOI: 10.1016/j.blre.2007.05.002

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

G6PD deficiency: the genotype-phenotype association.PMID 17611006Read ↗

Glucose-6-phosphate dehydrogenase deficiency: correlation between the genotype, biochemistry and phenotype.Semantic proximity Read ↗

Glucose-6-phosphate dehydrogenase deficiencySemantic proximity Read ↗

Genetic variants causing G6PD deficiency: Clinical and biochemical data support new WHO classificationSemantic proximity Read ↗

Pathogenic G6PD variants: Different clinical pictures arise from different missense mutations in the same codonSemantic proximity Read ↗

Glucose-6-Phosphate Dehydrogenase: Update and Analysis of New Mutations around the World.Semantic proximity Read ↗

Chronic non-spherocytic haemolytic disorders associated with glucose-6-phosphate dehydrogenase variants.Semantic proximity Read ↗

Glucose-6-Phosphate Dehydrogenase Deficiency.Semantic proximity Read ↗

G6PD: Population genetics and clinical manifestationsSemantic proximity Read ↗

G6PD deficiency: global distribution, genetic variants and primaquine therapy.Semantic proximity Read ↗

New WHO classification of genetic variants causing G6PD deficiencySemantic proximity Read ↗

[Glucose-6-phosphate dehydrogenase deficiency and hereditary hemolytic anemia].Semantic proximity Read ↗

G6<scp>PD</scp> deficiency: a classic example of pharmacogenetics with on‐going clinical implicationsSemantic proximity Read ↗

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