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

Epidemiological shift of glucose-6-phosphate dehydrogenase mutations in northern Italy in the last 15 years.

Annals of hematology - 1 Nov 2021

Duca Lorena, Nava Isabella, Tavazzi Dario, Marcon Alessia, Motta Irene, Graziadei Giovanna

Abstract excerpt

Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an X-linked recessive hemolytic anemia caused by mutations in G6PD gene. The distribution and frequency of genetic variants differ depending on ethnicity and geographical areas. Because of new migrations different variants are now present in Europe. This retrospective study aims to identify variants among the G6PD deficient subjects referred since 2004 to...

Read the complete abstract on PubMed

Topics

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

Share to Africa South of the Sahara
Share to Asian People

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

Share to Emigrants and Immigrants

Share to Glucosephosphate Dehydrogenase

Share to Glucosephosphate Dehydrogenase Deficiency

Share to Mediterranean Region

Share to White People

Source

Identifiers

PMID: 34533603
DOI: 10.1007/s00277-021-04630-9

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

Epidemiological shift of glucose-6-phosphate dehydrogenase mutations in northern Italy in the last 15 years.PMID 34533603Read ↗

Practical approach for characterization of glucose 6-phosphate dehydrogenase (G6PD) deficiency in countries with population ethnically heterogeneous: description of seven new G6PD mutants.Semantic proximity Read ↗

G6PD Potenza: A Novel Pathogenic Variant Broadens the Mutational Landscape in the Italian PopulationSemantic proximity Read ↗

G6PD Potenza: A Novel Pathogenic Variant Broadening the Mutational Landscape in the Italian Population.Semantic proximity Read ↗

Glucose-6-phosphate dehydrogenase deficiency in Italian blood donors: prevalence and molecular defect characterization.Semantic proximity Read ↗

Incidence and complete molecular characterization of glucose-6-phosphate dehydrogenase deficiency in the Guangxi Zhuang autonomous region of southern China: description of four novel mutations.Semantic proximity Read ↗

Glucose-6-phosphate dehydrogenase deficiency in Portugal: biochemical and mutational profiles, heterogeneity, and haplotype association.Semantic proximity Read ↗

Molecular heterogeneity of glucose-6-phosphate dehydrogenase (G6PD) variants in Italy.Semantic proximity Read ↗

G6PD deficiency: the genotype-phenotype association.Semantic proximity Read ↗

Multiple G6PD mutations are associated with a clinical and biochemical phenotype similar to that of G6PD Mediterranean.Semantic proximity Read ↗

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

Glucose-6-phosphate dehydrogenase deficiency in northern Mexico and description of a novel mutation.Semantic proximity Read ↗

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

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