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

The first reported case of G6PD deficiency due to Seoul mutation in Poland.

Annals of hematology - 1 May 2014

Kaczorowska-Hac Barbara, Burzynska Beata, Plochocka Danuta, Zak-Jasinska Katarzyna, Rawa Katarzyna, Adamkiewicz-Drozynska Elzbieta

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 Child
Share to Erythrocyte Transfusion
Share to Glucosephosphate Dehydrogenase
Share to Glucosephosphate Dehydrogenase Deficiency

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hyperbilirubinemia

Share to Mutation

Share to Poland

Share to Republic of Korea

Source

Open in PubMed Open full text

Identifiers

PMID: 24022758
DOI: 10.1007/s00277-013-1899-6
PMCID: PMC3976505

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The first reported case of G6PD deficiency due to Seoul mutation in Poland.PMID 24022758Read ↗

Identification of a case of glucose-6-phosphate dehydrogenase deficiency with G6PD Mediterranean-Middle East subtype in China.Semantic proximity Read ↗

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

G6PD deficiency.Semantic proximity Read ↗

Gene symbol: G6PD. Disease: Glucose-6-phosphate dehydrogenase deficiency.Semantic proximity Read ↗

Novel human pathological mutations. Gene symbol: G6PD. Disease: glucose-6-phosphate dehydrogenase deficiency.Semantic proximity Read ↗

Novel human pathological mutations. Gene symbol: G6PD. Disease: glucose-6-phosphate dehydrogenase deficiency.Semantic proximity Read ↗

A Novel de novo Mutation in the G6PD Gene in a Korean Boy with Glucose-6-phosphate Dehydrogenase Deficiency: Case Report.Semantic proximity Read ↗

G6PD Canton a common deficient variant in South East Asia caused by a 459 Arg----Leu mutation.Semantic proximity Read ↗

Genetic Profiles of Korean Patients With Glucose-6-Phosphate Dehydrogenase DeficiencySemantic proximity Read ↗

Molecular identification of mutations in G6PD gene in patients with favism in IranSemantic proximity Read ↗

[Novel PKLR gene mutation related erythropyruvate kinase deficiency: a case report].Semantic proximity Read ↗

G6PD Kalyan and G6PD Kerala; two deficient variants in India caused by the same 317 Glu-->Lys mutation.Semantic proximity Read ↗

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